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 act as a primary liaison to ensure project objectives and timelines are met.
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 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 Central Risk Manager provides subject matter expertise for monitoring strategies and collaborates with cross-functional teams to identify and mitigate project risks. They ensure data quality and integrity through remote data review and statistical monitoring while maintaining compliance with regulatory standards.
Provide project support and administrative coordination across multiple clinical initiatives, including patient engagement and recruitment strategies. Collaborate with cross-functional teams to support study execution while leveraging AI tools to improve team efficiency.
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 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/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 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 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 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 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 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 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 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.
Provide project and operational support to the clinical team while assisting with clinical project coordination and administrative tasks. Collaborate with cross-functional stakeholders to ensure study-related processes and documentation are managed effectively.
The Site Activation Specialist is responsible for managing site activation processes, including regulatory submissions and essential document collection. They also support site selection, feasibility, and the negotiation of investigator contracts and budgets.
The specialist will set up, maintain, and close out project files and study information while managing financial reports and key performance indicators. They will also facilitate internal and external meetings and provide support for quality assurance and audit activities.
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.
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 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 CRA will conduct on-site and remote monitoring of clinical research studies to ensure compliance with protocols and data integrity. They will also contribute to process development, provide mentorship to junior staff, and collaborate with cross-functional teams to support clinical trial execution.
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 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 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.
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 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 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 Clinical Data Reviewer performs specialized clinical data reviews ahead of significant project milestones to ensure data readiness and validity. They work as an extension of the clinical scientist to identify inconsistencies, highlight errors, and manage queries across large, multi-faceted data sets.
The CRA will perform site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They will also manage site-level activities, verify clinical data accuracy, and support patient recruitment and retention strategies.
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 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 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 Project Specialist manages study documentation, including regulatory files and Trial Master Files, while providing administrative support to project leads. They facilitate effective communication among team members and site staff and assist with quality assurance activities and audit preparations.
The Clinical Trial Manager 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 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 ensure the safety and integrity of clinical study data.
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 patient recruitment and retention strategies.
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 Clinical Operations Specialist assists clinical monitoring staff with site management activities and ensures compliance with study protocols and guidelines. They are also responsible for maintaining the Trial Master File, tracking clinical documentation, and coordinating site supplies.
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 CRA II 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 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 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 Sr. Clinical Trial Manager provides medical and scientific leadership to ensure high-quality execution of clinical trials within the assigned region. They act as a bridge between clinical development and cross-functional teams to ensure regulatory compliance and patient safety.
The Associate Project Manager is responsible for managing project deliverables, including vendor oversight, risk mitigation, and tracking study performance. They also handle financial reporting, budget monitoring, and ensure all study activities comply with GCP and regulatory standards.
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 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 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 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 Clinical Medical Advisor provides country-level and global clinical leadership for trials, ensuring adherence to regulatory standards and protocol integrity. They collaborate with cross-functional teams to optimize trial execution, manage risks, and communicate medical insights to internal and external stakeholders.
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 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 manager is responsible for leading and developing a team of Clinical Data Scientists while overseeing project performance, quality, and financial health. They serve as the primary point of contact for client relationships and ensure all project deliverables meet regulatory and internal quality standards.
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 Clinical/Medical Scientist develops medical plans and performs 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.
The Clinical Trial Assistant supports clinical monitoring staff with site management activities and ensures compliance with study protocols and regulatory guidelines. They are responsible for maintaining the Trial Master File, tracking clinical documentation, and coordinating site supplies and team meetings.
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 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 Clinical/Medical Scientist develops medical plans and performs 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 data integrity are maintained.
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 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 patient recruitment and retention strategies.
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 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 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.
Manages the negotiation and execution of clinical study agreements and investigator budgets while ensuring compliance with sponsor and company requirements. Serves as a subject matter expert to resolve global contracting issues and provides strategic guidance to internal and external stakeholders.
The Lead Contract Manager will oversee complex contract negotiations and lifecycle management within the clinical solutions environment. They will collaborate with cross-functional teams to deliver innovative solutions that meet customer needs and support drug development goals.
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.
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.
Perform site management activities in compliance with SOPs, regulatory guidelines, and study protocols to ensure audit readiness. Manage site-level communication, data review, and investigator training while supporting patient recruitment and retention strategies.
The specialist is responsible for encoding adverse events, medical history, and medications using industry-standard dictionaries like MedDRA and WHOdrug. They also collaborate with clinical and data management teams to ensure coding consistency and timely processing of project data.
The Principal Medical Writer will lead clinical documentation efforts and manage complex regulatory submissions. They will collaborate with cross-functional teams to ensure high-quality deliverables that meet customer needs and regulatory standards.
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.
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.
The Central Monitor II supports the Central Monitoring Lead in maintaining data analytical tools and conducting risk-based quality management (RBQM) reviews. They identify data quality trends, manage site performance issues, and communicate findings to the study team.
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 central and local regulatory submissions, facilitate communication between investigational sites and functional leads, and support budget and contract negotiations.
The Senior Director is responsible for driving sales growth across a geographic territory by balancing new client acquisition with the expansion of existing accounts. They lead multi-functional solution development and maintain strong relationships with key stakeholders to maximize territory performance.
The Regulatory Affairs Manager will lead and support regulatory submissions and life-cycle management procedures within Latin American markets. They will act as a local regulatory expert, coordinating strategy and ensuring compliance with regional health authority requirements.
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 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 clinical trial lifecycle.
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 patient recruitment and retention strategies.
The CRA II 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 maintain essential study documentation.
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 Clinical Research Coordinator will lead study start-up activities, manage clinic logistics, and ensure all clinical trials are conducted in compliance with protocols and GCP regulations. They are responsible for participant recruitment, data entry, monitoring safety, and coordinating with sponsors and project managers throughout the study lifecycle.
The CRA II 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 safety and data integrity throughout the study lifecycle.
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 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 Site Activation Specialist oversees the end-to-end site activation process at the country level, ensuring compliance with project requirements and regulatory standards. They manage submissions to regulatory authorities and ethics committees, negotiate site contracts and budgets, and maintain essential documentation.
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 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 role involves overseeing the end-to-end site activation process at the country level, including regulatory submissions and essential document collection. It also requires monitoring project timelines, financial aspects, and ensuring compliance with SOPs and local regulatory requirements.
The Research Nurse will coordinate and complete subject trial visits while ensuring all procedures and assessments are performed according to protocol and SOPs. They are responsible for maintaining accurate documentation, administering trial medication, and reporting adverse events to the site team and project management.
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 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.
The CRA I performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They also manage site-level activities, conduct source document reviews, and maintain accurate clinical data in tracking systems.
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.
The manager will support the execution of global regulatory CMC strategies for marketed products and contribute to the preparation of regulatory documentation. They will also serve as a primary regulatory contact and collaborate with cross-functional teams to manage submissions.
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.
Responsible for site management oversight, clinical monitoring, and ensuring protocol, GCP, and regulatory compliance. Collaborates with functional leaders to coordinate study milestones, manage risks, and oversee clinical team deliverables.
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 Clinical Trial Manager is responsible for site management oversight, clinical monitoring, and ensuring protocol, GCP, and regulatory compliance. They coordinate study milestones, manage project risks, and oversee the performance of CRAs and Central Monitors to ensure data integrity and patient safety.
The Clinical Trial Manager is responsible for site management oversight, clinical monitoring, and ensuring protocol, regulatory, and GCP compliance. They coordinate with functional teams to meet study milestones, manage risks, and oversee the performance of CRAs and Central Monitors.
The CRA II/SCRA 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 Project Coordinator will build and institutionalize project management frameworks while providing strategic oversight for regulatory portfolios. They will also facilitate communication between stakeholders and manage project documentation to ensure alignment with objectives and timelines.
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.
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 Senior Site Contracts Lead oversees the negotiation of clinical study agreements and investigator budgets while serving as a subject matter expert for global site contracting issues. They are responsible for establishing contract execution strategies, mentoring staff, and collaborating with internal and sponsor stakeholders to ensure study start-up goals are met.
The candidate will support client submissions to Health Canada for a portfolio of biologic and small molecule rare disease products. Responsibilities include managing life cycle submissions, coordinating responses to regulatory inquiries, and providing local regulatory intelligence.
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 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 guidance to site staff to ensure project objectives are met.
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 trial lifecycle.
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 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 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 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, processes, and SOPs while collaborating with cross-functional teams to support clinical trial operations.
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.
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.
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.
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.
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.
The consultant will support client submissions to Health Canada for a biologic and small molecule rare disease product portfolio. Responsibilities include managing life cycle submissions, coordinating Clarifax responses, and providing local regulatory intelligence.
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.
The Biometrics Optimization Lead manages project teams and oversees the development of standard operating procedures and training programs within the Biometrics business unit. They are responsible for driving end-to-end project governance, monitoring operational metrics, and mentoring staff to ensure successful clinical trial delivery.
The Associate Director will lead patient-focused drug development strategies by integrating the patient voice across the full clinical development lifecycle. They will drive global recruitment and retention initiatives while managing cross-functional collaboration to modernize the clinical trial experience.
The CRA II 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 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.
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 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 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 support patient recruitment and retention strategies.
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 Site Contracts Specialist manages the end-to-end process of negotiating and executing clinical trial agreements and budgets with study sites. They collaborate with internal teams and sponsors to ensure compliance, mitigate operational risks, and maintain accurate project documentation.
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 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 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.
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 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.
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.
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, documentation, and site operations.
The Clinical Research Associate is responsible for the full lifecycle of clinical studies, including site qualification, initiation, monitoring, and close-out visits. They ensure protocol compliance, data integrity, and regulatory adherence while managing site-level activities and communication.
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 Medical Scientist serves as a Clinical Data Reviewer, identifying data errors and performing ongoing reviews of clinical study participant data. They collaborate with cross-functional teams to ensure data quality, manage clinical data queries, and support audit readiness throughout the study lifecycle.
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.
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.
Perform site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. Manage site-level activities, data integrity, and communication to meet project objectives and timelines.
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.
Manage and execute clinical trial-related payments in accordance with contracts, regulatory requirements, and internal procedures. Collaborate with cross-functional teams and study sites to ensure efficient financial operations and timely payment execution.
The manager oversees data management and pharmacovigilance operations, including line management of staff and ensuring data quality and compliance. They are responsible for project coordination, budget management, and representing the safety department in client and project meetings.
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 maintain essential study documentation.
The 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-level activities, and ensuring subject safety and data integrity.
The Clinical Research Associate (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, maintain accurate clinical data, and act as a primary liaison between the sponsor and study sites.
The 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 maintain essential study documentation.
The Clinical Research Associate performs site qualification, initiation, monitoring, and close-out activities to ensure protocol and regulatory compliance. They also manage site-level activities, verify clinical data accuracy, and maintain essential study documentation.
The 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 maintain essential study documentation.
The Clinical Research Associate performs site qualification, initiation, monitoring, and close-out visits to ensure regulatory and protocol compliance. They are responsible for managing site-level activities, verifying clinical data accuracy, and maintaining essential study documentation.
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 while ensuring patient safety.
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 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 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 study documentation throughout the project lifecycle.
The Project Data Manager is responsible for overseeing all data management services for assigned projects, ensuring compliance with contractual agreements and sponsor expectations. They act as the functional lead, coordinating team activities, managing project finances, and ensuring all milestones are met according to SOPs and regulations.
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 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.
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.
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 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 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 Principal Biostatistician leads biomarker-related statistical activities across clinical studies, serving as the primary contact for sponsors. They are responsible for developing biomarker evaluation plans, conducting advanced data analysis, and mentoring junior staff to ensure high-quality deliverables.
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 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 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 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 while supporting subject safety and data integrity.
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 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 Statistical Programmer leads programming activities, develops custom code for clinical trial outputs, and ensures compliance with regulatory standards. They also mentor junior staff, manage project timelines, and serve as a technical subject matter expert for CDISC and regulatory submissions.
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 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 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 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 eCOA Project Manager will lead the end-to-end delivery of electronic Clinical Outcome Assessment solutions, serving as the primary liaison between sponsors, internal teams, and vendors. Responsibilities include managing study-specific project plans, overseeing system builds and UAT, and ensuring compliance with regulatory expectations throughout the clinical trial lifecycle.
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 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 provide mentorship to junior staff.
The Clinical Trial Manager is responsible for site management oversight, clinical monitoring, and ensuring protocol compliance and data integrity throughout the study lifecycle. They coordinate with cross-functional teams to meet study milestones, manage risks, and oversee the performance of clinical research associates and central monitors.
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 Regulatory Labeling Manager will support labeling negotiations with health authorities and interpret safety data to inform labeling updates. They are responsible for preparing labeling components for eCTD submissions and utilizing structured content authoring tools.
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 Regulatory Consultant will manage and track regulatory submissions while maintaining content plans within Veeva Vault RIM. They will also coordinate submission activities and translate project timelines into actionable plans using Smartsheet and Microsoft Project.
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 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 Project Manager II 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 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 Trial Manager is responsible for site management oversight, clinical monitoring, and ensuring protocol compliance and data integrity throughout the trial lifecycle. They coordinate with functional teams to meet study milestones, manage risks, and serve as an escalation point for investigator sites.
The Site Monitoring Lead is responsible for overseeing clinical monitoring, site management, and central monitoring deliverables to ensure patient safety and regulatory compliance. They manage study risks, coordinate with functional teams, and provide leadership to CRAs and Central Monitors to meet study milestones.
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.
The specialist administers contract management processes, including negotiating budgets and agreements for clinical trials at a project level. They also collaborate with internal and external stakeholders to ensure compliance with timelines, quality standards, and regulatory requirements.
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 medical scientist will collaborate with cross-functional teams to shape solutions that meet customer needs throughout the drug development and commercialization continuum. They are expected to take initiative and challenge the status quo to drive patient progress and customer success.
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 Project Data Manager will collaborate with cross-functional teams to deliver clinical solutions and support drug development processes. They are responsible for managing project data while ensuring compliance with industry standards and customer requirements.
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 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 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 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 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 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 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.
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 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 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.
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 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.
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 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 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 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 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 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 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.
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 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.
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 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.
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.
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.
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 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 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.
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.
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 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.
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, 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 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 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 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 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.
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 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 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.
