The Senior Site Contracts Manager is responsible for developing, negotiating, and managing US site budgets and clinical trial agreements for Pharma and Vaccine studies. They will lead cross-functional projects, ensure compliance with GCP, and maintain strong relationships with academic institutions and internal stakeholders.
Develop regulatory documents for global submissions in accordance with ICH guidelines and manage medical writing projects across cross-functional teams. Participate in process improvement initiatives and mentor junior medical writing staff to ensure high-quality deliverables.
Leads the preparation and completion of complex regulatory medical writing deliverables while ensuring scientific accuracy and adherence to regulatory standards. Coordinates cross-functional activities and mentors less experienced writers to ensure project timelines and budget requirements are met.
The Clinical Trial Manager will oversee clinical development projects to ensure the efficient delivery of therapies while maintaining high standards of quality. They will collaborate with cross-functional teams to streamline processes and achieve customer goals within a global environment.
The Site Activation Specialist II oversees the end-to-end site activation process at the country level, ensuring compliance with regulatory requirements and project timelines. They manage local submissions, essential document collection, and facilitate communication between investigational sites and functional leads.
The Registry Management Associate serves as the primary point of contact for patients and healthcare providers to support non-interventional clinical studies. They are responsible for managing study data, ensuring protocol adherence, and maintaining accurate documentation for real-world research.
The Project Manager oversees interdisciplinary clinical research studies, ensuring compliance with regulatory requirements and GCP standards. They are responsible for managing project timelines, budgets, and deliverables while acting as the primary liaison between the company and the customer.
Oversees the negotiation and execution of clinical study agreements and investigator budgets while providing subject matter expertise to internal and sponsor stakeholders. Manages contract execution strategies and ensures alignment with global study start-up plans and timelines.
The Sr Global Feasibility Lead independently manages RFP and paid feasibility objectives across various therapeutic areas while collaborating with internal stakeholders. They are responsible for researching scientific literature, developing site selection strategies, and providing evidence-based recommendations to support study success.
Responsible for clinical site management, monitoring deliverables, and ensuring protocol compliance and data integrity throughout the study lifecycle. Collaborates with cross-functional teams to manage study milestones, risk mitigation, and site interactions from activation to closeout.
The Clinical Data Reviewer will collaborate with cross-functional teams to manage and review clinical trial data within the oncology therapeutic area. They are responsible for applying deep expertise to understand customer needs and delivering solutions that accelerate drug development progress.
The Senior Clinical Research Associate performs site monitoring, management, and close-out activities to ensure regulatory and protocol compliance. They are responsible for verifying clinical data accuracy, protecting patient safety, and maintaining essential study documentation throughout the site lifecycle.
Conduct and document site qualification, initiation, monitoring, management, and close-out activities while ensuring compliance with protocols, regulations, and GCP requirements. Review clinical records and data, manage site issues and study documentation, support patient recruitment and audit readiness, and coordinate with study teams and sponsors.
The Research Nurse will coordinate and complete subject trial visits both on-site and off-site while ensuring adherence to trial protocols and SOPs. They are responsible for accurate data documentation, administration of trial medication, and the reporting of adverse events to the project management team.
Prepare, review, negotiate, and manage site-specific clinical trial contracts and budgets, coordinating with sponsors, sites, legal, finance, and clinical operations teams. Track contracting milestones and project finances, ensure quality and compliance, resolve operational risks, and provide guidance and training to colleagues.
Conduct site qualification, initiation, monitoring, management, and close-out activities while ensuring protocol, regulatory, and GCP compliance. Review clinical records and data, manage site documentation and investigational products, resolve issues, and support recruitment, audit readiness, and delivery of study timelines.
Develop regulatory documents for global submissions in accordance with ICH guidelines and manage medical writing projects across cross-functional teams. Mentor junior staff and participate in process improvement initiatives to ensure high-quality document preparation.
The Research Nurse will manage day-to-day clinical trial activities, including protocol adherence, data documentation, and patient care both on-site and off-site. They are responsible for administering trial medication, processing samples, and reporting adverse events to ensure patient safety and data integrity.
Conduct on-site and remote monitoring of clinical studies, ensuring compliance with protocols, informed consent requirements, Good Clinical Practice, and regulatory standards. Develop monitoring tools and documentation, manage assigned study processes, resolve issues, and collaborate with investigators, site staff, and cross-functional teams.
The Senior Clinical/Medical Scientist will collaborate with the Medical Director to develop medical plans and perform regular medical data reviews to identify risks and trends. They serve as the primary interface between internal teams, customers, and vendors to ensure project milestones and data integrity are maintained.
Provides leadership and oversight for clinical trial managers to ensure quality monitoring and site management activities. Manages project financial performance, risk mitigation strategies, and cross-functional collaboration to meet sponsor expectations.
Conduct and document clinical site qualification, initiation, monitoring, management, and close-out activities while ensuring compliance with protocols, regulations, and GCP requirements. Review site records and clinical data, manage risks and queries, support recruitment and audit readiness, and coordinate site activities to meet project timelines.
The role involves managing clinical trial agreements, site budget negotiations, and the full contract lifecycle with minimal oversight. You will collaborate with internal and external stakeholders to ensure contract execution and site activation timelines are met.
Manage site contract and budget negotiations, including drafting, reviewing, finalizing, and documenting Clinical Trial Agreements and amendments while following sponsor-approved language and escalation processes. Coordinate start-up activities and meetings, maintain accurate project trackers, align stakeholders on timelines, and proactively address contractual and operational risks.
Conduct on-site and remote monitoring of clinical studies, ensuring compliance with protocols, informed consent requirements, GCP, and applicable regulations. Develop monitoring tools and processes, document findings, manage assigned study activities, and collaborate with investigators, site staff, and cross-functional teams.
The Contract Manager is responsible for independently managing clinical trial agreements, amendments, and site budget negotiations. They will also collaborate with internal and external stakeholders to ensure contract execution and site activation timelines are met.
The Clinical Trial Manager is responsible for site management oversight, clinical monitoring, and ensuring protocol and regulatory compliance throughout the trial lifecycle. They coordinate with functional teams to meet study milestones, manage risks, and oversee the performance of CRAs and Central Monitors.
The Clinical Trial Manager oversees site interactions from activation through closeout, including patient recruitment and investigator payments. They are responsible for identifying protocol execution risks, managing study budgets, and ensuring clinical team compliance with monitoring strategies and regulatory standards.
The Senior Medical Writer leads the preparation of clinical documentation, including protocols, study reports, and regulatory submissions, while ensuring scientific accuracy and adherence to regulatory standards. They also coordinate cross-departmental reviews, mentor junior staff, and maintain strong relationships with clients and internal teams.
The Senior Project Manager will lead clinical projects by collaborating with cross-functional teams to meet customer goals. They are responsible for navigating complex drug development processes and applying deep expertise to deliver high-quality solutions.
The Senior Clinical Research Associate performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and provide mentorship to junior staff.
The Senior Clinical Research Associate performs site monitoring, management, and close-out visits to ensure regulatory and protocol compliance. They also oversee data integrity, manage investigational product inventory, and provide mentorship to junior staff.
The Senior CRA performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and provide mentorship to junior staff.
The Senior Statistical Programmer develops custom code to generate clinical trial outputs such as tables, listings, and graphs while ensuring quality standards. They also act as a lead programmer, directing team activities and mentoring junior personnel.
The Senior Clinical Programmer will design, write, and maintain clinical programming solutions while providing technical leadership and mentorship to team members. They are responsible for managing study-level deliverables, coordinating with project teams, and ensuring high-quality standards across multiple concurrent clinical studies.
The Clinical Research Associate performs site qualification, initiation, monitoring, and close-out activities to ensure regulatory and protocol compliance. They manage site-level activities, verify clinical data accuracy, and maintain essential study documentation throughout the study lifecycle.
The Senior CRA I performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and support patient recruitment and retention strategies.
The Senior Clinical Research Associate performs site qualification, initiation, monitoring, and close-out visits to ensure protocol and regulatory compliance. They manage site-level activities, verify clinical data accuracy, and support subject recruitment and retention strategies.
The Senior CRA performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and provide guidance to site staff to ensure project objectives are met.
Manage site contracts specifically for observational studies within a clinical research environment. Collaborate with cross-functional teams to ensure efficient delivery of clinical solutions and project milestones.
Lead interdisciplinary clinical research projects from study launch through closeout, ensuring quality, timelines, budget performance, and compliance with GCP, SOPs, and regulatory requirements. Coordinate project teams and study partners, manage deliverables and risks, maintain inspection readiness and TMF quality, and build client relationships.
Conduct and document site qualification, initiation, monitoring, management, and close-out activities while ensuring compliance with protocols, regulations, and GCP requirements. Manage site performance, data quality, investigational products, essential documents, communications, and timelines, while supporting audits, recruitment, and the training or mentorship of junior CRAs.
Leads and coordinates medical writing deliverables for clinical and regulatory documents, ensuring scientific accuracy, clarity, quality, and compliance with applicable guidelines and standards. Collaborates with clients and cross-functional teams, resolves review comments, mentors less experienced writers, and manages assigned work within project budgets and timelines.
Oversee site start-up deliverables and project lifecycle maintenance, including regulatory submissions and amendments, site agreements and budgets, country-specific applications, timelines, and Trial Master File documentation. Manage client and cross-functional coordination, project risks, scope, and budgets while ensuring quality, compliance, and delivery against contracted expectations.
Lead and coordinate medical writing deliverables for clinical studies and regulatory submissions, ensuring scientific accuracy, clarity, consistency, and compliance with applicable guidelines and templates. Manage client and cross-functional reviews, resolve comments, support quality and editorial processes, and mentor less experienced writers while meeting project timelines and budgets.
The Site Contracts Specialist manages the end-to-end contract process, including drafting, negotiating, and executing clinical trial agreements and budgets. They also collaborate with internal and external stakeholders to ensure compliance with legal and financial standards while mentoring junior team members.
Conduct on-site and remote monitoring of clinical research studies to ensure compliance with protocols and regulatory standards. Collaborate with cross-functional teams and investigators to manage study documentation and resolve operational issues.
Performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. Manages site-level activities, verifies clinical data accuracy, and supports subject recruitment and retention strategies.
The Project Specialist is responsible for planning, directing, and communicating clinical study timelines while ensuring milestones are met. They also oversee operational aspects of clinical trials, including vendor management, budget monitoring, and ensuring compliance with SOP and GCP regulations.
The Site Augmentation Lead serves as the primary point of contact for sponsor clients and sites, overseeing the day-to-day management and close-out of allocated Site Solutions projects. They are responsible for ensuring project compliance with regulatory requirements, managing study budgets, and leading site engagement and resource allocation strategies.
The Principal Statistical Programmer leads programming activities for clinical trials, including the development of summary tables, listings, and datasets. They also provide technical expertise, mentor junior staff, and ensure compliance with regulatory standards like CDISC.
Lead the development and implementation of publication strategies and produce high-quality scientific content including manuscripts and presentations. Manage external agencies, author collaborations, and budget milestones while ensuring compliance with publication policies.
The CRA II performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and support patient recruitment and retention strategies.
The Principal Clinical Programmer serves as a subject matter expert for core business packages and leads clinical programming projects. They are responsible for designing, validating, and maintaining software, as well as providing mentorship and technical guidance to the team.
Conduct and document clinical site qualification, initiation, monitoring, management, and close-out activities while ensuring protocol, regulatory, and GCP compliance. Manage site performance, data and investigational product oversight, issue escalation, study documentation, and coordination with project teams and site personnel.
The Senior CRA is responsible for performing site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and provide guidance to site staff to ensure project objectives are met.
The Senior Project Data Manager is responsible for the end-to-end project management of data management services for assigned clinical projects. They act as the primary liaison between internal functional groups and sponsors to ensure deliverables meet contractual agreements and regulatory standards.
Lead Site Augmentation projects from handover through closeout, managing sponsor and site relationships, resources, budgets, documentation, training, timelines, and regulatory compliance. Coordinate site engagement and contracting, monitor performance and risks, and ensure project deliverables meet client expectations and applicable clinical standards.
Develop, validate, and quality-check statistical programming outputs and datasets in accordance with statistical analysis plans, specifications, sponsor requirements, and applicable regulatory guidelines. Lead programming activities, monitor deliverables and timelines, review project documentation, communicate with project teams and sponsors, and mentor other programming staff.
The CRA II performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They manage site-level activities, verify clinical data accuracy, and support subject recruitment and retention strategies.
The Clinical Operations Specialist assists clinical monitoring staff with site management activities and ensures compliance with corporate policies and study protocols. They are also responsible for maintaining the Trial Master File, tracking clinical documentation, and coordinating team meetings.
The Project Manager II oversees interdisciplinary clinical research studies, ensuring compliance with GCP and regulatory requirements while managing project timelines and budgets. They act as the primary liaison between the company and the customer to ensure successful study launch, conduct, and closeout.
The specialist is responsible for managing country-level regulatory and ethics committee submissions throughout the clinical trial lifecycle. They serve as the primary point of contact for regulatory authorities and provide strategic guidance to project teams to ensure compliance and timely delivery.
The specialist is responsible for managing country-level regulatory and ethics committee submissions throughout the clinical trial lifecycle. They serve as the primary point of contact for regulatory authorities and ensure all activities comply with local regulations and project timelines.
The Site Activation Manager II is responsible for leading and managing Site Start-Up deliverables within assigned projects to ensure sites are activation-ready on time and within budget. They oversee all activities from site selection through life cycle maintenance, including regulatory submissions and budget management.
The role involves performing site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. It also requires managing site-level activities, verifying clinical data accuracy, and supporting subject recruitment and retention strategies.
Conduct on-site and remote monitoring of clinical research studies to ensure compliance with protocols and regulatory standards. Collaborate with cross-functional teams and investigators to manage site activities, documentation, and study progress.
The Clinical Research Associate performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They manage site-level activities, verify clinical data accuracy, and support patient recruitment and retention strategies.
The Senior Clinical Research Associate performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and provide guidance to site staff to ensure project objectives and timelines are met.
Administers contract management processes including negotiating and preparing clinical trial contracts and budgets at a project level. Collaborates with internal and external stakeholders to ensure compliance with timelines, legal requirements, and budgetary standards.
Oversee site management, clinical and central monitoring, and study team delivery to ensure patient safety, protocol and regulatory compliance, data integrity, and achievement of study milestones. Manage monitoring plans, systems, training, resourcing, documentation quality, risks, client updates, and inspection readiness, escalating and mitigating issues as needed.
Manage assigned clinical study sites throughout the study lifecycle, including site identification, qualification, start-up, remote and on-site monitoring, documentation, and compliance with applicable procedures and regulations. Support data quality, patient recruitment and retention, audit readiness, site training, and timely communication and issue resolution with site staff and project teams.
Oversee site management, clinical and central monitoring, study team resourcing, and clinical deliverables to ensure patient safety, regulatory and protocol compliance, data integrity, and achievement of study milestones. Coordinate with clients and cross-functional teams, manage risks and escalations, maintain study systems and documentation, and support inspection readiness and data lock deadlines.
Plan, coordinate, and manage Phase 1 clinical studies, including protocols, schedules, budgets, resources, milestones, and stakeholder updates. Ensure compliance with GCP and applicable regulations, maintain accurate study documentation, resolve study issues, and support team members.
Develop medical review plans with the Medical Director, review clinical data to identify risks and trends, author and resolve medical queries, and support patient profile, safety, and protocol deviation reviews. Coordinate medical data and eligibility review across study teams, customers, and vendors while managing deliverables, timelines, quality, and compliance.
The role involves managing all aspects of clinical research studies, including site oversight, protocol execution, and coordination with investigators and internal teams. You will be responsible for tracking study progress, ensuring regulatory compliance, and mitigating risks to maintain data integrity and project timelines.
Responsible for site management oversight, clinical monitoring, and central monitoring deliverables to ensure patient safety and regulatory compliance. Collaborates with cross-functional teams to manage study milestones, risk mitigation, and project budget adherence.
The Contract Navigator manages the end-to-end contracting process, coordinating between internal stakeholders and external parties to ensure efficient execution. They provide strategic guidance, identify risks, and resolve issues to maintain compliance and project timelines.
The specialist is responsible for processing and triaging Individual Case Safety Reports (ICSRs) while ensuring data accuracy and regulatory compliance. They also perform literature screening, medical coding, and maintain safety tracking systems to support clinical trials and post-marketing programs.
The Study Manager oversees interdisciplinary clinical research studies, ensuring compliance with GCP and regulatory requirements while managing project timelines and budgets. They act as the primary liaison between the company and the customer to ensure successful study launch, conduct, and closeout.
Develop regulatory submission documents in accordance with global guidelines and manage medical writing projects across cross-functional teams. Participate in process improvement initiatives and mentor junior staff to ensure high-quality document delivery.
The Clinical Data Reviewer performs specialized clinical data reviews to ensure readiness for study milestones such as interim analysis and submissions. They identify data inconsistencies, raise queries, and monitor for safety signals while collaborating with cross-functional study teams.
Conduct on-site and remote monitoring of clinical research studies to ensure protocol adherence and data accuracy. Manage clinical trial processes, resolve data integrity issues, and provide mentorship to junior staff members.
The Principal Statistician leads clinical development plans, defines trial design strategies, and mentors biostatistics personnel. They oversee the preparation of statistical analysis plans and ensure high-quality deliverables throughout the clinical trial lifecycle.
The Senior Clinical Trial Manager will oversee global clinical studies, including protocol development, budget management, and vendor oversight. They are responsible for ensuring study timelines are met, managing site selection, and maintaining compliance with regulatory standards.
The Global Senior Clinical Trial Manager will oversee global clinical studies, managing vendor relationships, study budgets, and timelines. They are responsible for site selection, protocol development, and ensuring compliance with regulatory standards and clinical study plans.
The Global Senior Clinical Trial Manager is responsible for managing global clinical studies, including protocol development, budget oversight, and vendor management. They will lead study teams to meet project timelines, ensure regulatory compliance, and oversee site selection and patient recruitment strategies.
Develop and execute study and customer engagement strategies while leading pre-award activities and bid defense meetings. Manage cross-functional teams to ensure successful project delivery, financial performance, and adherence to regulatory standards.
The Principal Biostatistician will collaborate with cross-functional teams to provide statistical expertise across the drug development continuum. They are responsible for shaping solutions that meet customer needs while ensuring high-quality delivery in a complex clinical environment.
The Principal Biostatistician will perform exploratory analyses of clinical trial data using interactive R/Shiny applications to identify trends and safety signals. They will collaborate with cross-functional teams to define analytical requirements and translate complex statistical results into clear visual narratives.
The Central Report Reviewer is responsible for executing central report review activities to ensure patient safety, regulatory compliance, and data integrity. They review site monitoring documentation, assess risks, and escalate serious issues to the project management team.
The Project Manager II oversees interdisciplinary clinical research studies, ensuring compliance with regulatory requirements and GCP standards. They are accountable for project deliverables, financial performance, and maintaining strong client relationships to support study success.
The Principal Medical Writer leads the development of complex clinical documents and manages medical writing activities across various studies. They also provide expert peer review, ensure adherence to regulatory standards, and mentor less experienced team members.
Leads the preparation of complex medical writing deliverables and manages documentation strategy across clinical studies. Coordinates with cross-functional teams to ensure regulatory compliance and high-quality scientific output while mentoring junior staff.
The Project Specialist is responsible for planning and communicating clinical study timelines while ensuring milestones are met and projects remain within budget. They also oversee operational aspects of clinical trials, including site selection, vendor management, and ensuring compliance with regulatory standards.
The Clinical Trial Manager is responsible for site management oversight, clinical monitoring, and ensuring protocol compliance and data integrity throughout the trial lifecycle. They also manage project risks, coordinate with functional teams, and serve as an escalation point for site staff and investigators.
The Research Nurse will manage clinical trial protocols, ensure accurate data documentation, and coordinate subject visits both on-site and off-site. They are also responsible for administering trial medication, processing samples, and reporting adverse events in compliance with GCP standards.
The Clinical Trial Manager performs site qualification, initiation, monitoring, and close-out activities to ensure regulatory and protocol compliance. They are responsible for managing site-level activities, verifying clinical data accuracy, and supporting subject recruitment and retention strategies.
The CRA II performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and support subject recruitment and retention strategies.
The Senior Project Manager oversees interdisciplinary clinical research programs, ensuring compliance with regulatory requirements and GCP standards. They act as the primary liaison between the company and the customer to manage project deliverables, budgets, and timelines while leading the clinical team.
The manager will oversee quality assurance and regulatory compliance processes within the clinical solutions division. They will collaborate with cross-functional teams to ensure adherence to global regulatory standards and internal quality protocols.
The Clinical Research Associate performs site qualification, initiation, monitoring, and close-out visits to ensure protocol and regulatory compliance. They are responsible for managing site performance, verifying clinical data accuracy, and maintaining essential trial documentation.
The specialist is responsible for managing country-level site start-up activities, including regulatory submissions, ethics committee applications, and site activation processes. They also monitor project timelines, financial aspects, and ensure compliance with SOPs and local regulatory requirements.
The Senior Medical Writer leads the preparation of complex clinical documents such as protocols, study reports, and regulatory submissions while ensuring scientific accuracy and adherence to regulatory standards. They also coordinate cross-functional reviews, mentor junior staff, and maintain strong relationships with internal teams and clients.
The CRA II performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They manage site-level activities, verify clinical data accuracy, and maintain essential study documentation throughout the project lifecycle.
The Customer Contract Manager will own and manage complex contracts, change orders, and budgets while ensuring alignment with project scopes. They act as the primary customer contact to drive revenue targets and maintain effective relationships with internal and external stakeholders.
The Research Nurse will manage daily trial operations, including protocol adherence, data documentation, and patient assessments. They are also responsible for administering trial medication, processing samples, and reporting adverse events to the project team.
The Research Nurse will manage daily trial operations, including protocol adherence, data documentation, and patient assessments. They are responsible for administering trial medication, processing samples, and reporting adverse events to ensure patient safety and data integrity.
Performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. Manages site-level activities, verifies clinical data accuracy, and maintains essential study documentation.
The CRA II performs site qualification, initiation, monitoring, and close-out activities to ensure regulatory and protocol compliance. They manage site-level activities, verify clinical data accuracy, and act as a primary liaison between the study site and the project team.
Collaborate with cross-functional teams to plan, execute, and analyze biomarker aspects of clinical studies. Develop biomarker evaluation plans and provide statistical input using advanced AI and machine learning approaches.
The Patient Engagement Lead manages global clinical trial recruitment and retention strategies by collaborating with study teams and solution partners. They are responsible for overseeing project budgets, vendor performance, and the quality of patient engagement tactics to ensure enrollment goals are met.
The CRA performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and maintain essential study documentation.
The Senior Clinical Programmer designs, validates, and maintains clinical software using tools like SAS, Medidata, and Oracle to meet project specifications. They also lead programming activities across multiple studies, provide technical support to project teams, and manage change orders while ensuring high-quality deliverables.
Perform site monitoring, management, and close-out activities to ensure compliance with regulatory standards and study protocols. Manage site-level communication, data integrity, and investigational product reconciliation throughout the study lifecycle.
The CRA II is responsible for performing site qualification, initiation, monitoring, and close-out visits to ensure protocol and regulatory compliance. They also manage site-level activities, verify clinical data accuracy, and maintain essential study documentation.
The Principal Clinical Programmer designs, validates, and maintains clinical software while coordinating programming activities across multiple concurrent studies. They provide technical leadership, support, and subject matter expertise to project teams to ensure high-quality deliverables and adherence to specifications.
The Clinical Research Associate performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They manage site-level activities, verify clinical data accuracy, and maintain essential study documentation throughout the study lifecycle.
Collaborate with cross-functional teams to plan, execute, and analyze biomarker aspects of clinical studies. Develop biomarker evaluation plans and provide statistical input using AI and machine learning approaches.
The Director will build strategies to support customers through model evolution and develop new partnership models across FSP and FSO environments. They are responsible for translating delivery successes into value propositions and managing complex customer requirements.
The TMF Specialist is responsible for processing and reviewing safety documents in accordance with good documentation practices and TMF readiness criteria. They will also liaise with study owners to resolve document discrepancies and ensure overall TMF quality and completeness.
The consultant will independently author and manage CMC documentation for regulatory submissions across various global regions. They will also provide regulatory support for multidisciplinary project teams and ensure compliance with global regulatory requirements.
The CRA performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and support patient recruitment and retention strategies.
The CRA II/SCRA is responsible for performing site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and support subject recruitment and retention strategies.
The Site Contracts Specialist leads multi-country projects involving the negotiation and preparation of clinical trial agreements and investigator budgets. They also manage contract administration processes, ensure compliance with SOPs, and collaborate with internal and external stakeholders to resolve budgetary and legal issues.
The Senior CRA is responsible for performing site monitoring visits, ensuring regulatory and protocol compliance, and managing site-level activities to meet project objectives. They also oversee data integrity, investigational product accountability, and provide mentorship to junior staff.
The CRA II performs site qualification, initiation, monitoring, and close-out activities to ensure regulatory and protocol compliance. They manage site-level activities, verify clinical data accuracy, and support patient recruitment and retention strategies.
The Project Manager oversees interdisciplinary clinical research studies, ensuring compliance with regulatory requirements and GCP standards. They are responsible for managing project timelines, budgets, and deliverables while acting as the primary liaison between the company and the customer.
The Clinical Trial Manager II performs site qualification, initiation, monitoring, and close-out activities to ensure regulatory and protocol compliance. They manage site-level activities, verify clinical data accuracy, and support subject recruitment and retention strategies.
The CRA II/SCRA is responsible for performing site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and support subject recruitment and retention strategies.
The Global Site Activation Manager oversees all project start-up deliverables, including site selection, regulatory submissions, and the maintenance of clinical trial agreements. They are responsible for managing integrated timelines, budgets, and risk mitigation strategies while collaborating with cross-functional teams to ensure project success.
The Patient Concierge Coordinator manages travel logistics and reimbursement processing for patients in clinical trials. They serve as a primary point of contact for patient inquiries while ensuring compliance with study policies and data protection regulations.
The Clinical Trial Manager II oversees all aspects of clinical research studies, including site management, monitoring deliverables, and ensuring protocol compliance. They coordinate with cross-functional teams to meet study milestones while managing risks, budgets, and project timelines.
Manage patient travel logistics and reimbursement processing for clinical trial projects while collaborating with internal teams to implement support services. Serve as a primary point of contact for patients to resolve queries and ensure compliance with study-specific policies.
The Senior Statistical Programmer develops custom code to generate summary tables, listings, and graphs while ensuring quality standards and regulatory compliance. They also act as a lead programmer, directing project activities and mentoring junior personnel.
The Senior Clinical Research Associate performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They manage site-level activities, verify clinical data accuracy, and support subject safety and recruitment strategies.
The Principal Statistician will lead statistical activities for clinical trials, including the development of statistical analysis plans and oversight of project deliverables. They will also mentor biostatistics personnel and collaborate with sponsors to ensure high-quality, regulatory-compliant study results.
The Clinical Operations Specialist assists clinical monitoring staff with site management activities and ensures compliance with study protocols and regulatory guidelines. They are also responsible for maintaining the Trial Master File, tracking clinical documentation, and coordinating site supplies and team meetings.
The Clinical Research Associate is responsible for the full lifecycle of clinical trials, including site selection, initiation, monitoring, and close-out activities. They will manage investigator budgets, ensure compliance with trial protocols, and oversee the handling of clinical drug supplies at investigational sites.
The CRA II performs site qualification, initiation, monitoring, and close-out activities to ensure regulatory and protocol compliance. They also manage site-level communication, verify clinical data accuracy, and support subject recruitment and retention strategies.
The role involves partnering with clinical scientists to lead the clear and accurate completion of medical writing deliverables, specifically focusing on protocols and protocol amendments. The writer will manage medical writing activities, coordinate reviews, and ensure compliance with regulatory standards and client requirements.
The lead statistical programmer will develop custom code for summary tables, listings, and datasets while directing the programming activities of other personnel. They are responsible for ensuring quality standards, managing project timelines, and providing technical expertise on CDISC and regulatory requirements.
The Site Activation Specialist is responsible for managing site activation activities, including regulatory submissions and site feasibility support at the country level. They ensure project deliverables meet timelines, track milestones, and facilitate communication between investigational sites and functional leads.
The CRA II performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and support patient recruitment and retention strategies.
The Senior CRA is responsible for performing site qualification, initiation, monitoring, and close-out visits to ensure protocol and regulatory compliance. They also manage site-level activities, support patient recruitment, and ensure clinical data integrity throughout the study lifecycle.
The Assessment Scientist leads the scientific oversight of eCOA implementation, including UAT strategy and endpoint scale translation. They are also responsible for designing rater training programs to ensure standardized data collection and endpoint reliability across clinical sites.
The CRA II performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and support subject recruitment and retention strategies.
The role involves partnering with business development teams to identify opportunities, develop sales pipelines, and execute customer engagement plans for Patient Services. It also requires providing strategic leadership to align operational capabilities with market needs and driving cross-functional collaboration to ensure successful pursuit execution.
The Research Nurse will coordinate and conduct clinical trial visits, ensuring all procedures are performed according to protocol and relevant SOPs. They are responsible for accurate data collection, administration of trial medication, and reporting adverse events to the project management team.
The Regulatory Consultant will independently manage regulatory submissions, including INDs and product registrations, while providing strategic guidance and lifecycle management. They will act as a subject matter expert, collaborating with cross-functional teams to ensure compliance and drive regulatory initiatives.
The Project Manager oversees Clinical Surveillance & Training (CST) services to ensure scientific integrity and data quality throughout clinical trials. They manage project deliverables, coordinate with vendors and sponsors, and maintain study-specific documentation and training portals.
The Medical Writer II performs end-to-end scientific writing, including publication planning and document management within Veeva Vault. They also mentor less experienced writers and ensure all deliverables meet regulatory standards and client requirements.
The Research Nurse will coordinate and complete subject trial visits while ensuring all procedures and assessments are conducted according to protocol and SOPs. They are responsible for accurate data documentation, administration of trial medication, and reporting adverse events to the project management team.
The Clinical Research Associate performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They are responsible for verifying informed consent, managing clinical data integrity, and overseeing investigational product handling at assigned sites.
The Research Nurse will manage daily trial activities, including patient visits, protocol compliance, and accurate data documentation. They are also responsible for administering trial medication, processing samples, and reporting adverse events to the project management team.
The Research Nurse will coordinate and conduct clinical trial visits, ensuring all procedures and assessments are completed according to protocol and relevant SOPs. They are responsible for accurate data documentation, administration of trial medication, and the reporting of adverse events to the project management team.
The CRA performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and support subject recruitment and retention strategies.
The Project Associate drives the planning and execution of clinical trials while ensuring adherence to timelines and budgets. They also coordinate internal resources, manage project documentation, and provide mentorship to junior team members.
The CRA II is responsible for conducting on-site and remote monitoring of clinical research studies to ensure compliance with GCP and regulatory standards. They also contribute to the development of monitoring tools, SOPs, and collaborate with cross-functional teams to support clinical trial operations.
The Site Activation Specialist oversees the end-to-end site activation process, including regulatory submissions, essential document collection, and communication with competent authorities. They also manage site-specific contracts and budgets while ensuring compliance with project timelines and company SOPs.
The Site Activation Specialist is responsible for managing site activation deliverables at the country level, including regulatory submissions and site identification. They also oversee contract and budget negotiations while ensuring compliance with SOPs and project timelines.
The Clinical Trial Manager II is responsible for site management oversight, clinical monitoring, and ensuring protocol compliance and data integrity throughout the study lifecycle. They also manage study risks, coordinate with functional teams, and oversee the performance of CRAs and Central Monitors to meet project milestones.
The role is responsible for managing site start-up activities, including regulatory submissions, essential document collection, and site activation at the country level. It also involves negotiating site contracts and budgets while ensuring compliance with SOPs and regulatory requirements.
The Clinical Project Manager oversees interdisciplinary clinical research programs, ensuring compliance with GCPs and regulatory requirements while managing project timelines and budgets. They act as the primary liaison between the company and the customer, leading clinical teams and facilitating project delivery from launch to closeout.
Conduct on-site and remote monitoring of clinical research studies to ensure compliance with protocols and regulatory standards. Collaborate with cross-functional teams and investigators to manage study documentation and resolve operational issues.
Leads the preparation and completion of complex clinical medical writing deliverables while ensuring scientific accuracy and regulatory compliance. Coordinates cross-functional activities and mentors junior staff to ensure projects are delivered on time and within budget.
The manager will oversee a portfolio of life sciences companies, guiding opportunities from lead generation through qualification using AI-driven tools. They will also collaborate with internal teams to develop proposals, manage client relationships, and maintain accurate sales data in Salesforce.
The Project Manager oversees interdisciplinary clinical research studies, ensuring compliance with GCP and regulatory requirements while managing project timelines and budgets. They act as the primary liaison between the company and the customer to ensure successful study delivery and foster strong client relationships.
The Site Care Partner performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and support subject recruitment and retention strategies.
The CRA II performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and support subject recruitment and retention strategies.
The research nurse will conduct mobile clinical research visits directly in patients' homes, performing procedures such as phlebotomy, injections, and specimen collection. They are responsible for maintaining accurate clinical data and ensuring compliance with study protocols and ICH-GCP standards.
The Project Manager will provide operational expertise to support clinical program strategies, including site training, patient enrollment, and engagement activities. They will partner with cross-functional teams to manage project deliverables, maintain internal systems, and ensure compliance with clinical documentation standards.
The Senior Medical Writer leads the preparation of complex clinical and regulatory documents while ensuring scientific accuracy and adherence to regulatory standards. They also coordinate cross-functional reviews, mentor junior staff, and manage client relationships to ensure project deliverables are met on time and within budget.
The Project Associate drives and supports clinical trial project management activities, including coordination of tasks, timelines, and budgets. They ensure project execution through stakeholder communication, documentation, and adherence to quality assurance standards.
The lead statistical programmer will develop custom code for summary tables, listings, and datasets while ensuring quality standards and regulatory compliance. They will also direct programming activities, mentor junior staff, and serve as a technical subject matter expert for CDISC standards.
The Research Nurse will manage daily trial operations, including subject visits, medication administration, and accurate data documentation according to protocols. They will also facilitate patient recruitment, report adverse events, and maintain effective communication with the project team and investigators.
Leads the preparation and completion of complex medical writing deliverables such as clinical study reports, protocols, and regulatory submissions. Coordinates cross-functional reviews and ensures all documentation adheres to regulatory standards and client requirements.
Execute commercial lifecycle management strategies and regulatory submissions with a focus on US, Canada, and EU markets. Participate in cross-functional teams and serve as the primary regulatory CMC contact for assigned products.
The Senior Statistical Programmer develops custom code to generate summary tables, listings, graphs, and derived datasets while ensuring quality standards. They also act as a lead programmer, directing activities, mentoring personnel, and collaborating with biostatisticians to resolve project discrepancies.
Conduct on-site and remote monitoring of clinical research studies to ensure compliance with protocols and regulatory standards. Collaborate with cross-functional teams and investigators to manage site visits, track study progress, and ensure accurate documentation.
The Central Monitor II performs remote patient data review for clinical research to ensure compliance with protocols, ICH-GCP, and regulatory requirements. They identify safety concerns, document observations, and escalate issues to the project team to maintain data integrity.
The Senior Clinical Trial Manager is responsible for site management oversight, clinical monitoring, and ensuring protocol and regulatory compliance throughout the study lifecycle. They manage project risks, coordinate with cross-functional teams to meet study milestones, and oversee the performance and training of clinical team members.
Develop custom programming code using SAS to generate summary tables, listings, and graphs according to statistical analysis plans. Act as a lead statistical programmer to direct programming activities, ensure quality standards, and mentor junior personnel.
The Senior Clinical Research Associate performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and support subject recruitment and retention strategies.
The Senior Clinical Project Manager will lead and oversee Phase I and early development clinical trials from study start-up through closeout. They are responsible for managing project timelines, budgets, and cross-functional teams while ensuring compliance with regulatory standards and sponsor requirements.
The Senior Principal Biostatistician will collaborate with cross-functional teams to provide expert statistical support across the drug development continuum. They will apply deep therapeutic and technical expertise to shape innovative solutions that meet complex customer needs.
The Clinical/Medical Scientist will develop medical plans and perform regular medical data reviews to identify risks and trends in infectious disease clinical trials. They will also serve as a primary interface between internal teams, customers, and vendors to ensure project milestones and quality deliverables are met.
Conduct on-site and remote monitoring of clinical research studies to ensure compliance with protocols and regulatory guidelines. Manage project components, including site visit coordination, documentation of monitoring activities, and collaboration with cross-functional teams.
Performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. Manages site-level activities, verifies clinical data accuracy, and maintains essential study documentation throughout the lifecycle.
The Site Activation Specialist II oversees the end-to-end site activation process at the country level, ensuring compliance with project requirements and regulatory timelines. They are responsible for managing submissions to regulatory authorities and ethics committees, as well as negotiating site contracts and budgets.
The Clinical Research Associate performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They manage site-level activities, verify clinical data accuracy, and maintain essential documentation throughout the study lifecycle.
The specialist is responsible for managing site activation processes, including regulatory submissions, contract negotiations, and budget management at the country level. They also act as a subject matter advisor for clinical trial regulatory intelligence and ensure compliance with company SOPs and local legislation.
The Site Activation Specialist is responsible for managing site activation activities, including regulatory submissions, site identification, and contract/budget negotiations. They ensure compliance with project requirements, SOPs, and timelines while maintaining accurate documentation in the Trial Master File.
The Regulatory Publishing Senior Manager is responsible for creating, assembling, and delivering electronic submissions to global health authorities. They lead publishing activities at a portfolio level while ensuring compliance with industry standards and health authority requirements.
The Manager FSP 360 is responsible for managing multifunctional team members, ensuring project deliverables are met, and maintaining strong relationships with internal and external stakeholders. They act as a Syneos Health ambassador, overseeing performance, compliance, and resource management to drive customer success and business growth.
The manager will support the execution of global regulatory CMC strategies for marketed and development products, including the preparation of regulatory documentation. They will provide guidance to cross-functional teams to ensure compliance with global regulatory requirements and support product compliance topics.
The Senior Project Manager is responsible for leading the operational, financial, and strategic execution of clinical research projects from proposal to final delivery. They act as the primary client liaison, managing cross-functional teams to ensure studies are completed on time, within budget, and in compliance with regulatory standards.
The Clinical Trial Manager performs site qualification, initiation, monitoring, and close-out activities to ensure regulatory and protocol compliance. They also manage site-level activities, oversee data integrity, and support subject recruitment and retention strategies.
The Principal Clinical Programmer provides technical leadership and subject matter expertise for clinical programming projects, including study build, system integrations, and application administration. They also oversee program-level operations, mentor junior staff, and manage vendor relationships to ensure high-quality, timely deliverables.
Responsible for site management oversight, clinical monitoring, and central monitoring deliverables to ensure patient safety and regulatory compliance. Collaborates with cross-functional teams to manage study milestones, risk mitigation, and clinical project team performance.
The CRA I performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They are responsible for verifying clinical data accuracy, managing site-level activities, and ensuring patient safety and data integrity throughout the study lifecycle.
The Director of Clinical Development Operations leads the technical strategy for the FSP Enablement Team and manages clinical operations to ensure quality and efficiency standards are met. They are responsible for line management, process optimization, and ensuring compliance with GCP and ICH guidelines across the business unit.
The CRA II/Sr CRA I is responsible for performing site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, maintain essential study documentation, and support subject recruitment and retention strategies.
Conduct on-site and remote monitoring of clinical research studies to ensure compliance with protocols and regulatory standards. Collaborate with cross-functional teams and investigators to manage study operations and ensure accurate documentation of monitoring activities.
The Senior Biostatistician will review statistical analysis plans, develop analysis datasets, and provide statistical support for clinical pharmacology and Phase I studies. They are responsible for validating statistical outputs and ensuring all documentation complies with regulatory and CDISC standards.
The CRA performs site qualification, initiation, monitoring, and close-out activities to ensure regulatory and protocol compliance. They manage site-level activities, verify clinical data accuracy, and support subject recruitment and retention strategies.
The Senior CRA II performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and support subject recruitment and retention strategies.
The Adult Research Nurse will manage daily trial operations, including protocol adherence, data documentation, and patient assessments. They will also coordinate trial visits, administer medication, and ensure accurate reporting of adverse events while maintaining effective communication with the research team.
The role involves providing expert guidance on Risk-Based Quality Management (RBQM) and central monitoring activities to ensure clinical trial compliance and data integrity. You will collaborate with cross-functional teams to identify risks, define quality tolerance limits, and oversee the resolution of issues identified through data analytics.
Design and execute real-world evidence studies using EMR and claims data to support clinical development, HEOR, and regulatory strategy. Collaborate cross-functionally to translate complex analytical results into actionable insights for decision-making.
The Research Nurse will conduct clinical trial visits at patient homes and clinical sites, ensuring all procedures follow trial protocols and SOPs. They are responsible for accurate data documentation, administration of trial medication, and reporting adverse events to the project management team.
The Medical Scientist is responsible for ensuring the integrity and quality of clinical data through rigorous safety surveillance and protocol-defined study monitoring. They will assist the lead clinician with data interpretation, safety narrative preparation, and the management of clinical study documentation.
The Clinical Programmer II designs, writes, validates, and maintains software using tools like SAS, Oracle RDC, and Medidata Rave to meet clinical study specifications. They also lead programming activities, coordinate project deliverables, and provide technical guidance to team members.
The Project Manager oversees interdisciplinary clinical research studies, ensuring compliance with regulatory standards and contractual agreements. They lead project teams to manage quality, timelines, and budgets while acting as the primary liaison between the company and the customer.
The role involves managing site activation activities, including regulatory submissions, contract negotiations, and budget management at the country level. It also requires ensuring compliance with SOPs, maintaining Trial Master File documentation, and providing subject matter expertise for clinical trial regulatory processes.
The Clinical Research Associate performs site qualification, initiation, monitoring, and close-out visits to ensure compliance with regulatory standards and study protocols. They manage site-level activities, verify clinical data accuracy, and maintain essential study documentation to support project objectives.
The Senior Medical Writer leads the preparation of complex clinical documents, ensuring scientific accuracy and adherence to regulatory standards. They also coordinate cross-departmental activities, mentor junior staff, and manage client relationships to ensure deliverables are completed on time and within budget.
The Principal Biostatistician leads statistical activities across multiple studies, serving as the primary sponsor contact and providing expert consultancy on study design and protocol development. They also oversee project deliverables, mentor junior staff, and ensure compliance with regulatory standards throughout the clinical trial lifecycle.
The CRA II performs site qualification, initiation, monitoring, and close-out activities to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and support subject recruitment and retention strategies.
The Regulatory Consultant will manage and track regulatory submissions while maintaining content plans within Veeva Vault RIM. They will also translate project timelines and coordinate communication between internal teams and regulatory publishing departments.
The Principal Statistical Programmer leads programming activities, develops custom code for clinical trial outputs, and ensures compliance with regulatory standards like CDISC. They also mentor junior staff, manage project timelines, and serve as a technical subject matter expert for biostatistics teams.
The CRA II performs site qualification, initiation, monitoring, and close-out activities to ensure regulatory and protocol compliance. They manage site-level activities, verify clinical data accuracy, and maintain essential trial documentation throughout the study lifecycle.
The Project Manager will collaborate with cross-functional teams to navigate complex drug development and commercialization processes. They are responsible for understanding customer needs and delivering innovative solutions to ensure project success.
The Principal Statistical Programmer develops custom code to generate summary tables, listings, and datasets while ensuring quality standards and regulatory compliance. They also act as a lead, directing programming activities, mentoring personnel, and providing technical expertise on CDISC standards.
The Principal Statistical Programmer will lead programming activities for clinical trials, including the development of ADaM datasets, tables, listings, and figures. They will also provide technical expertise, mentor junior staff, and ensure compliance with regulatory standards and project timelines.
The Project Manager provides guidance and daily oversight for the management of international clinical trials, ensuring adherence to budgets and timelines. They also manage CRO interactions, oversee study conduct from start-up to close-out, and coordinate data review processes.
The CRA II performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and support patient recruitment and retention strategies.
The Site Contracts Lead manages the end-to-end contract process, including drafting, negotiating, and executing clinical trial agreements and budgets. They also provide functional guidance to team members, ensure compliance with SOPs, and act as a liaison between internal departments and external sites.
The Senior Manager will lead cross-functional regulatory project management activities for global submissions, ensuring compliance with FDA, EMA, and ICH guidelines. They are responsible for managing multiple marketing applications and lifecycle management submissions from initial filing through to final approval.
The Regulatory Labeling Manager is responsible for the development, maintenance, and oversight of labeling content for mature pharmaceutical products. This includes authoring labeling documents, ensuring regulatory compliance, and collaborating with cross-functional teams to align on labeling changes.
The Clinical Operations Specialist assists clinical monitoring staff with site management activities and ensures compliance with study protocols and regulatory guidelines. They are also responsible for maintaining the Trial Master File, tracking clinical documentation, and coordinating site supplies.
The Executive Director of Strategic Business Development drives enterprise-level sales growth by managing global account strategies and securing high-impact partnerships. They collaborate cross-functionally to develop client-centric solutions and navigate complex procurement environments within the biopharmaceutical sector.
The Director of Business Development is responsible for driving sales growth across a geographic territory by balancing new client acquisition with the expansion of existing accounts. This role involves orchestrating multi-functional solution development and maintaining strong relationships with key stakeholders in the biopharmaceutical industry.
The Clinical Research Associate performs site qualification, initiation, monitoring, and close-out activities to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and support subject recruitment and retention strategies.
The Medical Scientist works with the Medical Director to develop medical plans and perform regular medical data reviews to identify risks and trends. They also serve as the primary interface between internal teams, customers, and vendors to ensure project milestones and quality deliverables are met.
Develop and validate SDTM/ADaM datasets and TLFs while supporting safety and efficacy analyses for clinical trials. Lead cross-functional teams and contribute to e-submissions ensuring full CDISC compliance.
The Project Manager is responsible for overseeing trial master file management, coordinating study deliverables across departments, and managing vendor relationships. They also handle financial reporting, risk mitigation strategies, and facilitate team training to ensure project milestones are met.
The role involves overseeing the site activation process, managing regulatory submissions, and ensuring quality deliverables at the country level. It also includes supporting site selection, contract negotiation, and maintaining regulatory intelligence in compliance with SOPs.
The role involves leading the preparation of complex regulatory medical writing deliverables while ensuring scientific accuracy and adherence to regulatory standards. The writer will coordinate cross-functional activities, mentor junior staff, and manage client relationships throughout the document development process.
The Site Activation Specialist is responsible for managing site start-up activities, including regulatory submissions, contract negotiations, and budget management at the country level. They ensure compliance with SOPs and project requirements while tracking milestones and providing contingency plans for potential delays.
The Research Nurse will manage day-to-day trial activities, including protocol compliance, data documentation, and patient assessments. They are also responsible for administering trial medication, processing samples, and reporting adverse events to the project team.
The Project Manager oversees interdisciplinary clinical research studies, ensuring compliance with regulatory requirements and GCP standards. They are responsible for managing project timelines, budgets, and deliverables while acting as the primary liaison between the company and the customer.
The Senior Central Risk Manager provides subject matter expertise for monitoring strategies and collaborates with cross-functional teams to identify and mitigate project risks. They ensure compliance with protocols, ICH/GCP standards, and regulatory requirements while managing study deliverables and budget expectations.
The specialist manages resource solutions for specific roles, ensuring data integrity within global resourcing tools and trackers. They analyze capacity and skillsets to support assignment recommendations and facilitate communication between internal stakeholders and business units.
Administers contract management processes including negotiating budgets and contracts for clinical trials while ensuring compliance with protocols and legal standards. Collaborates with internal and external stakeholders to facilitate contract execution and provides functional guidance to team members.
The Principal Medical Writer leads the development of complex medical writing deliverables and manages documentation strategy across clinical studies. They also mentor junior staff, ensure compliance with regulatory standards, and collaborate with cross-functional teams to meet client objectives.
The Associate Director will oversee central monitoring activities to ensure clinical trial success and operational excellence. They will collaborate with cross-functional teams to shape solutions that meet customer needs and drive patient progress.
The CRA II is responsible for conducting on-site and remote monitoring of clinical research studies to ensure compliance with protocols and regulatory standards. They also contribute to the development of monitoring tools, SOPs, and collaborate with cross-functional teams to support clinical trial operations.
The Senior Clinical Trial Operations Specialist will manage project files, regulatory documentation, and study information while ensuring effective communication across the project team. They will also provide administrative support to project leads and assist with quality assurance activities, including audit preparation and documentation.
The Project Data Manager acts as the functional lead for data management, coordinating team activities and ensuring project milestones are met according to SOPs and regulations. They are also responsible for financial management, resource planning, and maintaining project documentation to support internal and external audits.
The CRA II performs site qualification, initiation, monitoring, and close-out activities to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and maintain essential study documentation throughout the clinical trial lifecycle.
Perform site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. Manage site-level activities, verify clinical data accuracy, and maintain investigator site files while ensuring subject safety and data integrity.
The CRA performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and maintain essential study documentation throughout the project lifecycle.
The CRA performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and support subject recruitment and retention strategies.
The Senior Clinical Trial Manager is responsible for site management oversight, clinical monitoring, and ensuring protocol compliance and data integrity. They lead clinical project teams, manage study risks, and coordinate with functional leaders to meet study milestones and deliverables.
Provide leadership to clinical operations within the APAC region to ensure the overall delivery and performance of clinical trials. Collaborate with cross-functional teams to navigate drug development complexities and meet customer goals.
The biostatistician will design and execute real-world evidence studies using EMR and claims data to support clinical development, HEOR, and regulatory strategy. They will apply robust statistical methodologies and collaborate cross-functionally to translate complex analytical results into actionable insights.
The Senior Clinical Research Associate performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and support subject recruitment and retention strategies.
The Site Contracts Manager will negotiate and manage clinical trial budgets and agreements with academic institutions and clinical sites. They will also lead contracting projects, ensure compliance with GCP, and proactively manage risks to maintain study timelines.
The manager provides leadership for the operational and financial aspects of clinical trial supplies throughout the project life cycle. They are responsible for vendor management, inventory planning, and ensuring compliance with regulatory standards and study requirements.
The project manager will lead the execution of oncology and cell & gene therapy trials from startup through closeout while serving as the primary point of contact for sponsors. They are responsible for managing study timelines, budgets, regulatory compliance, and cross-functional team coordination to ensure inspection readiness.
The Clinical Project Manager will lead the end-to-end execution of complex Phase 2b inflammation studies, managing timelines, deliverables, and cross-functional teams. They are responsible for vendor oversight, risk mitigation, and ensuring all study documentation and operational milestones are met from start-up through closeout.
The CRA II performs site qualification, initiation, monitoring, and close-out activities to ensure regulatory and protocol compliance. They also manage site-level activities, verify clinical data accuracy, and support subject recruitment and retention strategies.
The Research Nurse will manage daily trial operations, including protocol adherence, data documentation, and subject visits. They are responsible for administering trial medication, processing samples, and reporting adverse events to the project management team.
The statistician provides support across the project lifecycle, from protocol development to clinical study reports, while coordinating biostatistics and programming activities. They serve as a biostatistics representative on project teams, ensuring high-quality deliverables and adherence to regulatory standards.
The Medical Writer II manages end-to-end scientific writing workflows, including publication planning and Veeva Vault document management. They also mentor less experienced writers and ensure all deliverables meet regulatory and client standards.
The Clinical Scientist collaborates with the Medical Director to develop medical plans and perform rigorous medical data reviews to identify risks and trends. They serve as the primary interface between internal teams and customers to ensure project milestones and quality deliverables are met.
Responsible for the development, coordination, and implementation of Phase 1 clinical research studies, including site management and monitoring oversight. The role involves tracking study progress against milestones, managing resource allocation for CRAs, and ensuring regulatory compliance and data integrity.
The role is responsible for overseeing site management, clinical monitoring, and regulatory compliance to ensure patient safety and data integrity. It involves coordinating with functional leaders to meet study milestones and managing the performance of CRAs and Central Monitors.
Lead the migration to SAS Viya and provide high-level technical expertise in statistical programming to generate summary tables, listings, and datasets. Mentor team members and ensure all deliverables comply with industry standards and regulatory requirements.
The role involves developing custom SAS code to generate summary tables, listings, and datasets according to statistical analysis plans. As a lead programmer, the candidate will direct programming activities, ensure quality standards, and mentor junior personnel.
Perform site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. Manage site-level activities, verify clinical data integrity, and maintain the Investigator Site File and Trial Master File.
The CRA is responsible for performing site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They manage site-level activities, verify clinical data integrity, and maintain the Investigator Site File.
Lead pre-award strategy and commercial leadership for Real World Late Phase (RWLP) accounts, including RFP strategy and budget structures. Serve as the strategic account leader post-award to maintain portfolio performance and sustain senior-level sponsor relationships.
Perform site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. Manage site-level activities, verify clinical data accuracy, and maintain the Investigator Site File and Trial Master File.
Develop custom programming code using SAS to generate summary tables, listings, and datasets according to statistical analysis plans. Act as the lead statistical programmer by directing personnel, reviewing project documentation, and ensuring quality standards are met.
Oversee site management, clinical monitoring, and central monitoring deliverables to ensure patient safety and regulatory compliance. Coordinate with functional leaders to meet study milestones and manage the clinical project team's contractual obligations.
Administers all contract management processes for clinical trials, including negotiating budgets and preparing agreements for investigators and vendors. Collaborates with legal and finance departments to ensure compliance with timelines and quality standards.
Manage quality assurance and regulatory compliance within the clinical solutions team to accelerate drug development. Collaborate with cross-functional teams to ensure customer success and adherence to healthcare regulations.
Provides medical oversight and monitoring for assigned clinical studies, serving as the primary medical contact for customers. Responsible for protocol design, drug safety oversight, and delivering therapeutic training to project teams.
Develop custom SAS programming code to generate summary tables, listings, and datasets according to statistical analysis plans. Act as a lead statistical programmer by directing activities, reviewing project documentation, and ensuring CDISC compliance.
The role involves performing site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. It also requires managing site-level activities, verifying clinical data integrity, and overseeing investigational product inventory.
Lead and manage Site Start-Up (SSU) deliverables globally or regionally to ensure study sites are activation-ready on time and within budget. Oversee the entire lifecycle from site selection and regulatory submissions to the collection of essential documents.
Perform site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. Manage site-level activities, verify clinical data integrity, and maintain the Investigator Site File.
The CRA performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They are responsible for verifying clinical data integrity, managing investigational products, and maintaining the Trial Master File.
The CRA is responsible for performing site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They manage site-level activities, verify clinical data integrity, and maintain the Investigator Site File.
The CRA is responsible for performing site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They manage site-level activities, verify clinical data integrity, and maintain the Investigator Site File.
Perform site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. Manage site-level activities, verify clinical data integrity, and maintain the Investigator Site File.
Perform site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. Manage site-level activities, verify clinical data accuracy, and provide guidance to site staff and junior CRAs.
The Employee Wellness Specialist focuses on enhancing employee well-being within a global life sciences services organization. The role involves collaborating with diverse teams to support a healthy and inclusive corporate culture.
Conduct on-site and remote monitoring of clinical research studies to ensure compliance with protocols and regulatory requirements. Develop quality monitoring tools and collaborate with cross-functional teams to support smooth clinical trial operations.
Responsible for hiring, managing, and developing biostatisticians while ensuring projects meet timelines, budgets, and quality standards. The role involves overseeing staff performance, mentoring associates, and managing client relationships to ensure successful project execution.
The role involves leading statistical activities across the clinical trial lifecycle, from protocol development to the final clinical study report. Responsibilities include mentoring biostatisticians, overseeing SAP preparation, and managing regulatory submission requirements.
Collaborate with Medical Directors to develop medical plans and perform regular medical reviews of data listings to identify risks and trends. Manage project scope and deliverables while interfacing between internal teams, customers, and vendors to ensure data integrity and subject safety.
Collaborates with Medical Directors to develop medical plans and perform regular medical reviews of data listings to identify risks and trends. Manages project scope and serves as the primary interface between internal teams, customers, and vendors regarding eligibility and data review.
Collaborate with Medical Directors to develop medical plans and perform regular medical reviews of data listings to identify risks and trends. Manage project scope and deliverables while interfacing between internal teams, customers, and vendors to ensure data integrity and subject safety.
Collaborate with Medical Directors to develop medical plans and perform regular medical reviews of data listings to identify risks and trends. Manage project scope and serve as the primary interface between internal teams, customers, and vendors regarding eligibility and data review.
Collaborate with Medical Directors to develop medical plans and perform regular medical reviews of data listings to identify risks and trends. Manage project scope and deliverables while interfacing between internal teams, customers, and vendors to ensure data integrity and subject safety.
Develop programs and provide statistical support for epidemiologists to source, organize, and interpret complex real-world data sets. Create analysis datasets, tables, and figures while ensuring outputs meet quality standards and protocol requirements.
Manage interdisciplinary clinical research studies ensuring compliance with GCP, SOPs, and regulatory requirements. Act as the primary liaison between the company and customers to oversee study launch, conduct, closeout, and financial performance.
The Study Manager oversees interdisciplinary clinical research studies, ensuring compliance with GCP and regulatory requirements while managing timelines and budgets. They act as the primary liaison between the company and the customer to ensure successful study launch, conduct, and closeout.
The Study Manager oversees interdisciplinary clinical research studies, ensuring compliance with GCP and regulatory requirements while managing timelines and budgets. They act as the primary liaison between the company and the customer to ensure successful study launch, conduct, and closeout.
Manage interdisciplinary clinical research studies ensuring compliance with GCP, SOPs, and regulatory requirements. Act as the primary liaison between the company and customers to oversee study launch, conduct, closeout, and financial performance.
Manage interdisciplinary clinical research studies ensuring compliance with GCP and regulatory requirements while acting as the primary liaison for customers. Lead project teams to oversee quality, timelines, budget management, and the completeness of the Trial Master File.
Manage interdisciplinary clinical research studies in oncology, ensuring compliance with GCP and regulatory requirements. Act as the primary liaison between the company and customers to oversee study launch, conduct, and financial performance.
Support the setup and maintenance of CTMS and TMF while managing study budgets and external service provider coordination. Perform central monitoring and data oversight to ensure the consistency and correctness of clinical study data.
Lead the negotiation and preparation of contracts and budgets for industry-sponsored clinical trials. Coordinate with legal, finance, and clinical operations to ensure accurate execution and archival of site-specific agreements.
The Director of Business Development is responsible for driving sales growth in a specific geographic territory through a mix of new client acquisition and existing account expansion. This involves developing tailored engagement plans and collaborating with cross-functional teams to deliver integrated life sciences solutions.
The Director of Business Development will lead initiatives to accelerate customer success in drug development and commercialization. This role involves collaborating with various teams to navigate complexities and drive impactful solutions for healthcare.
Lead business development efforts across the West Coast region to accelerate customer success in the life sciences sector. Partner with innovators to navigate the drug development and commercialization continuum.
The Director serves as a scientific subject matter expert in immunology, providing oversight for clinical trials and leading the development of global business opportunities. They coordinate with project managers to ensure study quality, manage budgets, and facilitate scientific advisory boards while producing technical reports and manuscripts.
The role serves as a scientific subject matter expert in oncology clinical trials, providing oversight for project proposals, study start-up, and ongoing management. It involves collaborating with business development to win global opportunities and leading the development of scientific reports, manuscripts, and study documentation.
The Director serves as a scientific subject matter expert in virology, providing oversight for clinical trials and leading the development of project proposals and bid defenses. They coordinate with project managers to ensure study quality, timelines, and budgets while facilitating scientific advisory boards and authoring industry publications.
The Sr CRA is responsible for site qualification, initiation, monitoring, and close-out visits, ensuring compliance with regulatory and protocol standards. They will assess site performance, manage site-level activities, and support patient recruitment and retention strategies.
The CRA II is responsible for performing site qualification, initiation, monitoring, and close-out visits, ensuring compliance with regulatory and protocol standards. They will also assess site performance and communicate any serious issues to the project team while supporting patient recruitment and retention strategies.
