The Clinical Trial Manager is responsible for overseeing country-level deliverables, maintaining project plans, and ensuring effective communication between global and local study teams. They also manage regional vendor oversight, drive recruitment, and ensure data cleaning standards are met.
Provides operational support across the full clinical site lifecycle including start-up, conduct, and close-out activities. Acts as a primary liaison between clinical teams, investigator sites, and external partners while managing essential study documentation and regulatory submissions.
Responsible for site management oversight, clinical monitoring, and central monitoring deliverables with a focus on patient safety and regulatory compliance. Collaborates with functional leaders to coordinate study milestones and ensures the clinical project team adheres to contractual obligations and study protocols.
The Clinical Operation Specialist assists clinical monitoring staff with site management activities and ensures compliance with study protocols and regulatory guidelines. They are also responsible for maintaining project files, tracking clinical data, and coordinating site supplies and team meetings.
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 ensure the safety and confidentiality of study subjects.
The CRA II performs site monitoring, management, and close-out activities to ensure regulatory and protocol compliance in oncology clinical trials. They are responsible for verifying clinical data accuracy, protecting patient safety, and managing site-level activities to meet project objectives.
The Senior 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, verify clinical data accuracy, and provide guidance to site staff to ensure project objectives are met.
The Clinical/Medical Scientist supports the Medical Director in developing medical plans and performing 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.
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 patient recruitment and retention strategies.
The Clinical Scientist collaborates 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 and customers to ensure project milestones and data integrity are maintained.
The specialist manages the end-to-end contract process for clinical trials, including drafting, negotiating budgets, and coordinating with legal and clinical teams. They also provide mentorship to junior staff and ensure compliance with departmental SOPs and project timelines.
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 Data Manager oversees data management activities for Phase I-III clinical trials to ensure quality, timeliness, and budget adherence. They act as the primary data management representative on multidisciplinary teams and manage clinical trial documentation and data review processes.
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 is responsible for processing and triaging Individual Case Safety Reports (ICSRs) while ensuring data accuracy and regulatory compliance. They also perform medical coding, literature screening, and maintain safety tracking systems in accordance with global regulations.
The Project Manager will collaborate with cross-functional teams to deliver clinical solutions and accelerate drug development processes. They are responsible for navigating complex project environments while ensuring customer needs are met through innovative strategies.
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 achieve project goals.
Responsible for site management oversight, clinical monitoring, and central monitoring deliverables with a focus on patient safety and regulatory compliance. Collaborates with functional leaders to coordinate study milestones and ensures the clinical team adheres to protocol and risk mitigation strategies.
The Project Financial Analyst serves as a financial partner to Business Unit Controllers by preparing, reconciling, and analyzing revenue, contracts, and project metrics. They are responsible for drafting variance analyses, managing project budgets in Oracle, and ensuring all financial reporting is accurate and timely.
The Senior Clinical Data Associate performs data management activities for Phase I-III clinical trials in accordance with ICH/GCP guidelines. Responsibilities include ongoing data review, reconciliation of third-party data and safety databases, and performing UAT and QC of clinical databases.
The Senior Clinical Data Associate performs activities for Phase I-III clinical trials to ensure data quality and adherence to timelines. Responsibilities include ongoing data review, reconciliation of third-party data, and performing user acceptance testing and quality control of clinical databases.
The Senior Clinical Data Associate performs data management activities for Phase I-III clinical trials, including data review and reconciliation. They are also responsible for conducting User Acceptance Testing (UAT) and Quality Control (QC) of clinical databases.
Perform ongoing clinical data review, including reconciliation of third-party data and serious adverse events. Conduct user acceptance testing and quality control of clinical databases while maintaining relevant documentation.
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.
The Senior Clinical Data Associate performs data management activities for Phase I-III clinical trials, including data review and reconciliation. They are also responsible for conducting User Acceptance Testing (UAT) and Quality Control (QC) of clinical databases.
The Senior Data Analyst will conduct longitudinal cohort studies and perform complex data analyses using SAS or R. They are responsible for assessing data quality, reviewing protocols, and ensuring adherence to data standards.
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 Regulatory Manager will lead regulatory activities, including the preparation of technical submissions and management of project timelines and budgets. They will act as a subject matter expert, providing strategic guidance and oversight to team members while ensuring compliance with global regulatory requirements.
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 Principal Medical Writer leads the development of complex clinical and regulatory documents while ensuring scientific accuracy and adherence to regulatory standards. They also manage document strategy, mentor junior staff, 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 Senior Central Risk Manager provides subject matter expertise for developing and updating risk-based monitoring strategies for clinical projects. They collaborate with cross-functional teams to identify, mitigate, and track risks while ensuring compliance with protocol, ICH/GCP, and regulatory standards.
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 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 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 provide guidance to site staff to ensure project objectives are met.
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.
The Global Trials Optimization Specialist manages program feasibility, recruitment, and retention planning to ensure successful clinical trial enrollment. They partner with cross-functional teams to identify enrollment challenges, monitor performance, and implement mitigation strategies throughout the trial lifecycle.
The Senior Project Specialist maintains and coordinates the logistical aspects of clinical projects while supporting functional leads to ensure project deliverables are met. They are responsible for managing study documentation, tracking key performance indicators, and facilitating communication between internal teams and external sponsors.
The specialist will identify and evaluate high-performing clinical sites while supporting feasibility assessments and enrollment planning. They will also collaborate with cross-functional teams and CROs to provide data-driven insights that influence global clinical trial strategy.
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 Senior Medical Scientist will collaborate with cross-functional teams to provide deep therapeutic expertise and clinical solutions. They will act with a drug development mindset to understand customer needs and drive progress across the commercialization continuum.
Provides operational support across the full clinical site lifecycle including start-up, conduct, and close-out activities. Acts as a primary liaison between clinical teams, investigator sites, and external partners while ensuring regulatory compliance.
The Clinical Trial Lead manages interdisciplinary clinical research studies, ensuring compliance with GCP and regulatory requirements while overseeing project timelines and budgets. They act as the primary liaison between the company and the customer to facilitate successful study launch, conduct, and closeout.
The Clinical Trial Leader is responsible for the end-to-end set-up, execution, and delivery of assigned clinical trials while ensuring compliance with GCP and regulatory standards. They lead interdisciplinary teams, manage project budgets, and act as the primary liaison between the company and the customer.
The specialist manages the end-to-end contract process for clinical trials, including drafting, negotiating budgets, and ensuring compliance with legal and protocol requirements. They also provide functional guidance, mentor junior staff, and collaborate with internal and external stakeholders to facilitate site start-up activities.
The Site Contracts Lead oversees the negotiation of clinical study agreements and investigator budgets while serving as a subject matter expert for internal and sponsor stakeholders. They are responsible for establishing contract execution strategies, managing escalations, and mentoring team members to ensure compliance with organizational standards.
The Site Contracts Specialist II 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 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 overseeing the end-to-end site activation process at the country level, including regulatory submissions and essential document collection. It also requires managing project timelines, budgets, and acting as a subject matter advisor for clinical trial regulatory requirements.
The CRA I performs site qualification, initiation, monitoring, and close-out activities to ensure regulatory and protocol compliance. They are responsible for verifying clinical data accuracy, managing site-level activities, and maintaining essential study documentation.
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.
Conduct on-site and remote monitoring of clinical research studies to ensure compliance with protocols and regulatory standards. Collaborate with cross-functional teams and site staff to manage project components and ensure accurate documentation of monitoring activities.
The Site Activation Specialist will manage the initiation and activation of clinical trial sites to ensure project timelines are met. They will collaborate with cross-functional teams to navigate complex regulatory and operational requirements in the drug development process.
The Site Contracts Specialist manages the negotiation and preparation of contracts and budgets for clinical trials, ensuring alignment with sponsor requirements. They also coordinate with internal and external stakeholders to streamline contract processes and maintain compliance with departmental SOPs.
The specialist will process and triage Individual Case Safety Reports (ICSRs) while ensuring data accuracy and regulatory compliance within safety databases. They will also perform literature screening, MedDRA coding, and maintain documentation for clinical trials and post-marketing programs.
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 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 support patient 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 findings.
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 facilitate study launch, conduct, and closeout.
The Manager of Site Contracts will oversee and manage clinical site contract processes to ensure efficient drug development operations. They will collaborate with cross-functional teams to navigate complex regulatory environments and meet project timelines.
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 provides mentorship to less experienced writers to ensure projects are delivered on time and within budget.
The CRA II performs site qualification, initiation, monitoring, and close-out activities to ensure compliance with regulatory standards and study protocols. They manage site-level activities, verify clinical data accuracy, and maintain essential study documentation throughout the trial 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 patient recruitment and retention strategies.
The Site Contract Specialist leads multi-country projects by negotiating and preparing site-specific 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 issues.
The role involves negotiating and managing site-specific clinical trial contracts and investigator budgets while ensuring compliance with regulatory standards. The specialist will also collaborate with internal and external teams to streamline processes and provide functional guidance on contract statuses.
Administer all contract management processes, including negotiating and preparing contracts, budgets, and related documents for clinical trials. Collaborate with internal and external legal, finance, and clinical operations departments to ensure compliance and timely execution of agreements.
The Clinical Trial Lead provides leadership and management for global clinical trials, ensuring quality execution and compliance with GCP and regulatory standards. They act as the primary liaison between the company and the customer while managing project budgets, timelines, and interdisciplinary teams.
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 support patient recruitment and retention strategies.
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 CRA I 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.
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 progress and ensure accurate documentation of monitoring activities.
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 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 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 CRA will perform 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 subject safety and data integrity throughout the study lifecycle.
The Senior Site Contracts Manager is responsible for negotiating clinical trial budgets and agreements while managing risks and ensuring compliance with sponsor requirements. They will lead contracting projects, collaborate with academic institutions, and drive process improvements to support operational excellence.
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 Pricing Systems Analyst will design and maintain VBA-based tools to automate budget costing and financial workflows. They will also collaborate with cross-functional teams to identify process inefficiencies and ensure data integrity across pricing systems.
The Senior Site Contracts Specialist manages the site identification process, including negotiating confidentiality agreements and site information forms. They also monitor site performance metrics and serve as the primary point of contact for investigative sites to ensure project compliance.
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 support subject recruitment and retention strategies.
The Senior 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 junior staff, and representing the programming team in sponsor meetings.
The role provides advanced functional and technical support for pharmacovigilance systems, serving as a senior point of contact for issue triage and resolution. It involves collaborating with IT, vendors, and business stakeholders to ensure system compliance, reliability, and operational continuity.
Leads the clear and accurate completion of medical writing deliverables while coordinating activities across departments. Manages document reviews, ensures adherence to regulatory standards, and mentors less experienced writers on complex projects.
The lead statistical programmer develops custom code for clinical trial outputs and ensures compliance with regulatory standards like CDISC. They also mentor junior staff, manage project timelines, and act as a technical subject matter expert for statistical programming activities.
The Principal Medical Writer leads the preparation of complex regulatory medical writing deliverables while ensuring scientific accuracy and adherence to regulatory standards. They also coordinate cross-functional reviews, mentor junior staff, and maintain strong relationships with clients and internal departments.
This position is responsible for leading clinical data management activities and providing support for global clinical trials. The role involves overseeing other clinical data associates, performing quality control, and ensuring data consistency across various clinical databases.
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 Clinical Trial Leader is responsible for the set-up, execution, and delivery of assigned clinical trials within the Evidence Network. They provide leadership and direction to the trial team to ensure efficient execution and accurate planning.
The Research Nurse will coordinate patient care and facilitate communication between patients and healthcare providers to ensure study protocol compliance. They are responsible for monitoring patient progress, collecting accurate data, and providing individualized support throughout the clinical research process.
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 customers to manage project deliverables, timelines, and budgets.
The Clinical Operations Specialist is responsible for ensuring site compliance with clinical protocols and maintaining accurate trial documentation. They also assist clinical monitoring staff with site management activities and coordinate essential project supplies and team meetings.
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 Sample Management Specialist I is responsible for the receipt, inventory, storage, and disposition of study samples and reference materials. They also assist in maintaining storage equipment and ensuring the integrity of materials through proper tracking and documentation.
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 Central Risk Manager will serve as a subject matter expert in RBQM and centralized monitoring, leading risk assessments and developing monitoring strategies for global clinical trials. They will partner with sponsors and cross-functional teams to drive data-driven decision-making and ensure study quality and patient safety.
Perform site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. 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 manage site-level activities, verify clinical data accuracy, and provide mentorship to junior staff while maintaining study timelines and budgets.
The Senior/Principal Medical Editor manages complex medical writing projects while ensuring documents meet regulatory standards and internal quality requirements. They also provide technical expertise, mentor staff, and contribute to process improvement initiatives.
The Medical Writer will collaborate with cross-functional teams to develop high-quality clinical and regulatory documents. They will apply deep therapeutic expertise to support drug development and commercialization efforts for global clients.
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 Project Manager oversees patient concierge projects from handover to completion, ensuring compliance with clinical SOPs and regulatory requirements. They manage project budgets, timelines, and vendor relationships while serving as the primary point of contact for clients and internal stakeholders.
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 Principal Statistician will lead statistical activities across the clinical trial lifecycle, including protocol development, statistical analysis plans, and regulatory submissions. They are also responsible for mentoring biostatistics staff, ensuring high-quality deliverables, and collaborating with sponsors and cross-functional teams.
The Senior CRA performs site qualification, initiation, monitoring, and close-out visits to ensure protocol compliance and data integrity. They manage site-level activities, verify informed consent, and ensure accurate clinical data capture while maintaining regulatory standards.
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 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.
Leads the preparation and completion of complex clinical medical writing deliverables while ensuring scientific accuracy and regulatory compliance. Coordinates cross-functional activities and provides mentorship to less experienced writers to ensure projects are delivered on time and within budget.
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.
Responsible for site management oversight, clinical monitoring, and central monitoring deliverables to ensure patient safety and regulatory compliance. Collaborates with cross-functional teams to meet study milestones, manage risks, and oversee clinical project team performance.
Leads the completion of medical writing deliverables, ensuring scientific accuracy and adherence to regulatory standards. Coordinates activities across departments and manages client comments to ensure projects are delivered on time and within budget.
The Project Financial Analyst II supports the Business Unit Controller by managing revenue recognition, project budgets, and financial forecasting within Oracle. They are responsible for drafting variance analysis reports, conducting project close-out reconciliations, and monitoring the overall financial health of assigned projects.
Manage and execute the site identification process while negotiating confidentiality agreements and site information forms. Serve as the primary point of contact for investigative sites and ensure compliance with all relevant regulations and project requirements.
The CRA 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 ensure the integrity of subject safety and data throughout the study lifecycle.
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 Principal Statistician oversees biostatistics personnel, develops training plans, and ensures the timely delivery of high-quality statistical outputs for clinical trials. They act as a lead biostatistician, collaborating with sponsors and regulatory agencies while ensuring compliance with SOPs and ICH guidelines.
The Senior CRA will perform on-site and remote monitoring visits to ensure regulatory, ICH-GCP, and protocol compliance for Phase I oncology trials. They are responsible for site management, source data verification, and escalating serious issues to the project team to ensure data integrity and patient safety.
The Medical Writer II performs end-to-end scientific writing, including managing publication plans and ensuring documents are MLR-ready for submission. They also mentor less experienced writers and collaborate across departments to ensure document accuracy and regulatory compliance.
The Medical Writer II manages end-to-end scientific writing workflows, including publication planning, journal submissions, and congress activity coordination. They ensure accurate documentation and adherence to regulatory standards while providing operational support to cross-functional teams.
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 Senior CRA 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 patient recruitment and retention strategies.
The Statistical Programmer II will collaborate with cross-functional teams to deliver clinical solutions and support drug development processes. They are responsible for applying technical expertise to meet customer needs and contribute to the successful execution of clinical studies.
The Clinical Trial Manager is responsible for site management oversight, clinical monitoring, and ensuring protocol, GCP, and regulatory compliance. They also manage study-specific risks, oversee clinical team deliverables, and coordinate with functional leaders to meet study milestones.
The Senior Statistical Programmer develops custom programming code for summary tables, listings, and graphs while ensuring quality standards and regulatory compliance. They also act as a lead programmer, directing activities for other personnel and participating in sponsor meetings.
The Site Contract 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 project timelines and regulatory standards.
The Project Financial Analyst II is responsible for preparing, reconciling, and analyzing business unit revenue, contracts, and project metrics. They support the Business Unit Controller by drafting financial forecasts, variance analyses, and ensuring accurate reporting within established timelines.
The Principal Medical Writer leads the development of complex clinical documents and manages medical writing activities across various studies. They also provide expert peer reviews, mentor junior staff, and ensure all deliverables meet regulatory and client standards.
The Clinical Research Associate (CRA) will perform site qualification, initiation, monitoring, and close-out visits to ensure protocol and regulatory compliance. They are responsible for managing site activities, verifying clinical data accuracy, and maintaining essential study documentation.
The role involves maintaining regulatory compliance for medical documents and representing the editorial group within study teams. It also includes managing project timelines, mentoring staff, and performing quality reviews to ensure adherence to industry standards.
The role involves copyediting and performing quality reviews on complex medical documents to ensure compliance with regulatory standards. Additionally, the editor will lead project deliverables, mentor staff, and provide technical expertise to cross-departmental study teams.
The Project Specialist will execute risk-based monitoring strategies and analyze clinical data to identify trends and potential risks. They will also collaborate with study teams to implement corrective actions and ensure regulatory compliance and patient safety.
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.
The CRA will perform site qualification, initiation, monitoring, and close-out visits to ensure protocol and regulatory compliance. They will also manage site-level activities, verify clinical data accuracy, and support patient recruitment and retention strategies.
The consultant will independently manage regulatory submissions, including gap analyses and technical documentation for global regulatory agencies. They will also act as a subject matter expert on multidisciplinary project teams to support product life cycle development and client interactions.
The 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 subject recruitment and retention strategies.
The 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 maintain essential trial documentation.
The project manager oversees medical writing deliverables, manages cross-functional teams, and ensures high-quality work products. They also supervise staff, handle performance reviews, and support business development activities such as proposal and budget preparation.
The Senior Medical Writer leads the preparation of complex clinical documents while ensuring scientific accuracy and adherence to regulatory standards. They coordinate cross-functional activities, mentor junior staff, and manage client relationships to ensure deliverables are completed on time and within budget.
The Senior Director serves as the lead scientific resource for Real-World Evidence (RWE) projects, providing executive oversight and driving business development opportunities. They are responsible for guiding scientific strategy, managing project delivery, and fostering relationships with sponsors and thought leaders.
Leads the preparation and completion of complex medical writing deliverables, ensuring scientific accuracy and adherence to regulatory standards. Coordinates cross-functional activities and mentors less experienced writers while managing client relationships and project timelines.
The Principal Research Scientist is responsible for developing, validating, and optimizing bioanalytical methods while coordinating laboratory activities. They also supervise and mentor scientific staff to ensure compliance with corporate policies and operational objectives.
The manager oversees interdisciplinary clinical research studies, ensuring compliance with GCP and regulatory standards while managing project budgets and timelines. They act as the primary liaison between the company and the customer to facilitate successful study launch, conduct, and closeout.
The role involves managing the end-to-end contract process for clinical trials, including drafting, negotiating, and executing site agreements and budgets. Additionally, the specialist will mentor junior staff and collaborate with internal and external stakeholders to ensure project timelines and quality standards are met.
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.
Lead the development of custom programming code to generate summary tables, listings, and graphs as specified in statistical analysis plans. Direct programming activities, monitor deliverables, and mentor junior programmers to ensure data accuracy and integrity.
The role involves performing site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. It also includes managing site-level activities, verifying clinical data integrity, and overseeing investigational product reconciliation.
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 clinical trial operations.
The role involves administering contract management processes and negotiating budgets and agreements for industry-sponsored clinical trials. It also requires coordinating with legal and clinical operations teams to ensure the accurate execution and archival of Clinical Trial Agreements.
The role involves leading and managing global clinical trials to ensure quality execution, compliance with GCP, and adherence to budgets and timelines. The Project Manager acts as the primary liaison between the company and the customer while overseeing interdisciplinary research studies.
Responsible for the development, coordination, and implementation of Phase 1 clinical research studies, including site management and monitoring oversight. The role involves managing project milestones, budgets, and ensuring protocol and GCP compliance while leading clinical team members.
Responsible for the development, coordination, and implementation of Phase 1 clinical research studies, including site management and monitoring oversight. The role involves managing clinical project teams, tracking study progress against milestones, and ensuring regulatory compliance and data integrity.
Responsible for the development, coordination, and implementation of Phase 1 clinical research studies, including site management and monitoring oversight. The role involves managing clinical teams, tracking project milestones, and ensuring protocol and regulatory compliance to maintain data integrity and patient safety.
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.
Leads the creation and accurate completion of medical writing deliverables, including protocols, clinical study reports, and regulatory submissions. Coordinates with cross-functional teams and clients to ensure scientific clarity and adherence to regulatory standards.
Leads the creation and completion of high-quality medical writing deliverables, including protocols, clinical study reports, and regulatory submissions. Coordinates with cross-functional teams and clients to ensure scientific accuracy and adherence to regulatory standards.
Coordinate care and facilitate communication between patients and healthcare providers for clinical research studies. Monitor patient progress and collect accurate data while ensuring compliance with regulatory standards and study protocols.
The role involves coordinating and completing clinical trial visits both on and off-site while ensuring strict adherence to trial protocols and SOPs. Responsibilities include administering medication, processing samples, and accurately reporting adverse events to the project management team.
The role involves coordinating and completing clinical trial visits both on-site and off-site while ensuring strict adherence to protocols and SOPs. Responsibilities include administering trial medication, processing samples, and accurately reporting adverse events to the project management team.
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.
The role is responsible for managing a multifunctional team to ensure quality deliverables and compliance with customer KPIs. It involves providing line management, overseeing professional development, and managing customer escalations.
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 collaborating with a Clinical Solutions team to shape drug development solutions that meet customer needs. The employee will work within a fully-integrated life sciences services organization to accelerate patient progress.
Leads the creation and accurate completion of regulatory medical writing deliverables, including protocols, clinical study reports, and NDA submissions. Coordinates with cross-functional teams and clients to ensure documents meet regulatory standards and are delivered on time and budget.
Responsible for site management oversight, clinical monitoring, and ensuring protocol and GCP compliance with a focus on patient safety and data integrity. The role involves managing clinical project teams, mitigating risks, and collaborating with functional leaders to meet study milestones.
Collaborate with Medical Directors to develop medical plans and perform regular medical reviews of data listings to identify risks and trends. Act as the primary interface between internal teams, customers, and vendors to ensure project milestones and data integrity are met.
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.
The role involves creating and updating payment trackers, processing invoices in GMS, and managing patient reimbursement costs. Additionally, the specialist is responsible for mentoring junior payment Clinical Trial Assistants.
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 role involves creating and updating payment trackers and processing invoices and payments within the GMS system. Additionally, the specialist manages patient reimbursement costs and provides mentoring to junior payment CTAs.
Administers contract management processes for clinical trials, including negotiating budgets and preparing site-specific contracts. Collaborates with legal, finance, and clinical operations to ensure timely execution and archival of agreements.
Lead the design and execution of epidemiological and data science projects to generate Real World Evidence for Oncology or Immunology. Develop study protocols, analysis plans, and regulatory documents while managing the identification of fit-for-purpose data sources.
The role involves managing site activation processes within a sponsor-dedicated environment to accelerate drug development. The specialist will collaborate with cross-functional teams to ensure efficient trial site setup and progress.
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 essential trial documentation.
Develop, negotiate, and execute Clinical Trial Agreements and budgets while managing financial aspects throughout the study lifecycle. Act as a key liaison between Clinical Operations, Finance, Legal, and investigative sites to ensure successful trial execution.
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 role involves performing site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. It also requires managing site-level activities, budgets, and timelines while acting as a primary liaison with project site personnel.
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.
Leads the creation and completion of complex medical writing deliverables, including protocols, clinical study reports, and regulatory submissions. Coordinates with cross-functional teams and clients to ensure scientific accuracy and adherence to regulatory standards.
Leads the creation and completion of complex medical writing deliverables, including protocols, clinical study reports, and regulatory submissions. Manages document strategies and coordinates activities across departments while mentoring junior medical writers.
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.
The role involves executing global regulatory CMC strategies and preparing documentation for small molecule products. It also provides regulatory guidance to cross-functional teams to ensure compliance with global requirements.
Provides medical oversight and monitoring for clinical studies in immunology and rheumatology, including protocol design and drug safety input. Leads medical responses for proposals and mentors staff on therapeutic research principles.
The Regulatory Device CMC Manager supports strategies for marketed and development products by preparing and submitting regulatory CMC documentation for combination devices. The role provides guidance to cross-functional teams to ensure global regulatory requirements are integrated into development and commercial programs.
The role focuses exclusively on processing and reviewing safety documents within the Trial Master File (TMF) system. Responsibilities include ensuring document completeness, indexing accuracy, and collaborating with study owners to resolve discrepancies.
The role involves serving as a statistical resource to mentor biostatisticians and oversee the preparation of Statistical Analysis Plans and clinical study reports. Additionally, the position focuses on maintaining R-based computing environments and developing Rshiny applications for data visualization.
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.
Oversees global salary structures, market pricing strategies, and job architecture to ensure competitiveness and consistency. Leads pay equity analyses and regulatory compliance while delivering sophisticated compensation analytics for executive leadership.
The role involves coordinating and completing subject trial visits both on- and off-site while ensuring adherence to trial protocols and SOPs. Responsibilities include administering trial medication, processing samples, and accurately reporting adverse events to the site team.
The role involves coordinating clinical trial visits and administering trial medications while ensuring accurate data collection in Case Report Forms. The nurse will also manage sample dispatch and report adverse events in compliance with SOPs and GCP guidelines.
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.
Provide statistical support to the Medical Affairs group focusing on exploratory analysis, observational studies, and real-world evidence. Manage the statistical lifecycle of projects from protocol development to the final clinical study report.
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.
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.
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 integrity, and maintain essential study documentation.
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 essential trial documentation.
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 maintaining the Investigator Site File.
Lead the operational and financial delivery of global clinical projects from proposal to final deliverables. Act as the primary liaison between the company and customers while managing interdisciplinary teams and ensuring regulatory compliance.
Perform site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. Manage site-level activities, data integrity, and investigator relationships while providing mentorship to junior CRAs.
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.
Develop custom programming code using R/RShiny to generate summary tables, listings, and graphs according to statistical analysis plans. Act as a lead programmer by directing activities, reviewing project documentation, and mentoring junior personnel.
The Medical Scientist will collaborate with clinical solutions teams to accelerate drug development and commercialization for customers. They will apply deep therapeutic expertise to shape solutions that improve patient progress and healthcare outcomes.
The role involves coordinating and completing clinical trial visits both on-site and off-site while ensuring strict adherence to protocols and SOPs. Responsibilities include administering trial medication, processing samples, and accurately reporting adverse events.
Perform site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. Manage site-level activities, data integrity, and subject safety for Real World Late Phase studies.
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.
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.
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.
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 developing custom SAS code to generate summary tables, listings, and graphs while ensuring compliance with statistical analysis plans and regulatory guidelines. The Principal Statistical Programmer also acts as a lead, directing programming activities and mentoring junior personnel.
The role is responsible for preparing SR&ED tax incentive claims and leading income and indirect tax audits. It also involves managing monthly, quarterly, and year-end closes while ensuring compliance with US and Canadian GAAP and Sarbanes-Oxley controls.
The Regulatory CMC Manager supports global regulatory CMC strategies for cell and gene therapy products during development and commercialization. This includes preparing regulatory documentation and providing guidance to cross-functional teams on compliance and GMP investigations.
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.
Provides comprehensive statistical support throughout the project lifecycle, from protocol development to the final clinical study report. Coordinates biostatistics and programming personnel to ensure high-quality deliverables and maintains inspection readiness.
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.
Perform remote patient data review for Phase I-IV clinical research to ensure protocol compliance and data integrity. Identify safety concerns and protocol deviations while communicating issues to the project team for action.
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.
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 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.
Lead the scientific oversight of eCOA implementation and manage the licensing, translation, and integrity of clinical outcome assessment scales. Design and deliver rater training programs to ensure standardized endpoint data collection across clinical sites.
Develop custom SAS code to generate summary tables, listings, and graphs according to statistical analysis plans. Act as a lead programmer by directing activities, reviewing project documentation, and mentoring junior personnel.
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.
Develop custom programming code using R or SAS to generate summary tables, listings, and datasets for clinical trials. Act as a lead statistical programmer, overseeing deliverables, ensuring CDISC compliance, and mentoring junior staff.
The role involves coordinating and completing subject trial visits both on- and off-site while ensuring adherence to trial protocols and SOPs. Responsibilities include administering trial medication, processing samples, and accurately reporting adverse events.
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.
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 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.
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 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.
Responsible for managing site activation and quality deliverables at the country level, including regulatory submissions and essential document collection. Acts as a subject matter advisor for in-country performance and supports site selection, contract negotiation, and budget management.
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.
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 role involves providing biostatistical expertise within the Clinical Pharmacology domain to accelerate drug development and commercialization. The Principal Biostatistician will collaborate with cross-functional teams to deliver data-driven solutions for healthcare customers.
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 Clinical Assessment Scientist will act as a COA Lead, collaborating with cross-functional teams to deliver clinical solutions for drug development projects. They will apply therapeutic expertise to understand customer needs and drive progress across the drug development continuum.
The Senior Clinical Research Associate 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 staff performance, and ensuring the safety and integrity of clinical trial data.
The CRA II performs 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 provide guidance to site staff to ensure project objectives are met.
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 trial documentation.
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.
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 trial documentation.
The Principal Site Grant Manager establishes and maintains investigator budget templates and negotiation strategies while serving as a subject matter expert for global site budgeting issues. They collaborate with internal and external stakeholders to ensure fair market value and operational compliance throughout the clinical trial budget life cycle.
The Clinical Trial Manager oversees site management, clinical monitoring, and central monitoring deliverables to ensure patient safety and regulatory compliance. They also manage study risks, coordinate with functional teams, and ensure adherence to contractual obligations and study timelines.
The CRA performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site performance, verify clinical data accuracy, and ensure patient safety and data integrity throughout the study.
Conduct on-site and remote monitoring of clinical research studies to ensure compliance with protocols and regulatory guidelines. Collaborate with cross-functional teams and investigators to support clinical trial operations and maintain accurate documentation.
The R Statistical Programmer will use R and SAS to develop custom code for generating summary tables, listings, graphs, and derived datasets according to the statistical analysis plan, ensuring outputs meet quality standards. This role involves performing validation programming, resolving discrepancies, managing project timelines, and acting as the lead statistical programmer directing the activities of other personnel.
The role involves using SAS or other software to develop custom programming code for generating summary tables, data listings, graphs, and derived datasets according to the statistical analysis plan and specifications. Responsibilities also include performing validation programming, ensuring outputs meet quality standards, and managing project timelines while acting as the lead statistical programmer.
The role involves performing site qualification, initiation, monitoring, management, and close-out visits while ensuring compliance with regulatory standards like ICH-GCP and protocol requirements. Key duties include evaluating site performance, managing data integrity via Source Document Review and query resolution, and maintaining essential study documentation.
The role involves performing all stages of site monitoring, including qualification, initiation, interim monitoring, management, and close-out visits, ensuring strict adherence to regulatory guidelines like ICH-GCP and protocol compliance. Key duties include evaluating site performance, verifying data accuracy via Source Document Review, managing query resolution, and ensuring proper handling and documentation of the Investigational Product.
The role involves performing site qualification, initiation, monitoring, management, and close-out visits, ensuring compliance with regulatory standards like ICH-GCP and protocol requirements. Responsibilities also include evaluating site performance, managing data integrity through source document review and query resolution, and maintaining essential study documentation.
The CRA II performs site qualification, initiation, monitoring, management, and close-out visits ensuring compliance with regulatory standards like ICH-GCP and protocol requirements. Responsibilities also include evaluating site performance, verifying informed consent, assessing patient safety and data integrity, and managing essential study documentation.
The Clinical Trial Manager II is responsible for oversight of site management, clinical monitoring, and central monitoring deliverables, focusing on patient safety, compliance, and data integrity from site activation through closeout. This role involves identifying and mitigating risks to trial deliverables, coordinating with other functional leaders, and ensuring quality control over monitoring documentation and study systems.
This posting is intended for a possible upcoming opportunity, adding interested candidates to a talent pipeline for future consideration as a Sr Clinical Trial Manager. The role involves working alongside industry experts to accelerate the delivery of important therapies to patients.
The job description focuses heavily on the company's mission, culture, and commitment to accelerating therapy delivery rather than listing specific IMS Specialist I tasks. The role is situated within a fully integrated biopharmaceutical solutions organization focused on clinical, medical affairs, and commercial insights.
The Clinical Research Associate (CRA) will perform 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 Principal Biostatistician serves as a resource for the statistical department, mentoring biostatisticians and overseeing training plans. They provide support across all statistical tasks during the project lifecycle and ensure high-quality work is completed on time.
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.
