Latest Clinical Research Associate Jobs

Director, Global Real-World Evidence & Health Outcomes Scientist, Oncology

This role involves planning and executing studies to generate robust health outcomes data for GSK's oncology products. The Director will collaborate with internal and external stakeholders to ensure evidence supports market positioning, reimbursement, and patient access. Key responsibilities include managing study timelines, ensuring deliverable quality, and translating customer needs into study concepts.

GSK United States

On-site Permanent

Director, Global Real-World Evidence & Health Outcomes Scientist, Oncology

This role involves planning and executing real-world evidence studies to support the launch and market positioning of GSK's oncology drugs. The Director will collaborate with internal and external stakeholders to ensure the generation of high-quality, scientifically credible evidence that meets regulatory and payer requirements.

GSK

On-site Permanent

Quality Oversight and Compliance Director

The Quality Oversight and Compliance Director will lead the development and maintenance of Quality Plans, ensure inspection and audit readiness, and provide quality oversight of process deviations and investigations. This role involves interpreting and applying regulatory requirements, identifying and mitigating compliance gaps, and driving continuous improvement in pan-regulatory processes and data quality.

Pfizer London, SW7 2AP, United Kingdom

On-site Permanent

Trial Vendor Senior Manager

This role involves managing all vendor-related aspects of global clinical trials, ensuring study outcomes are delivered on schedule, within budget, and to quality standards. You will collaborate closely with the Clinical Trial Team and vendor start-up managers, overseeing vendor interfaces, cost control, and service excellence.

Novartis United Kingdom

Hybrid Permanent Flexible

Senior Director, Head, Vaccines and Infectious Diseases, Global Epidemiology and RWE

This role involves providing strategic leadership in epidemiology, leading a global team of epidemiologists, and overseeing the design and execution of epidemiological studies. The position focuses on real-world data, cutting-edge methods, and technology to support vaccine and infectious disease research and development.

GSK

Hybrid Permanent

Senior Director, Head, Vaccines and Infectious Diseases, Global Epidemiology and RWE

This role involves providing strategic leadership in epidemiology, leading a global team of VID epidemiologists, and collaborating across R&D functions. Responsibilities include designing and executing epidemiological studies, contributing to regulatory submissions, and driving innovation in methodologies and tools.

GSK

Hybrid Permanent

Senior Director, Head, Vaccines and Infectious Diseases, Global Epidemiology and RWE

This role involves providing strategic leadership in epidemiology, leading a global team of VID epidemiologists, and collaborating across R&D functions. Responsibilities include designing and executing epidemiological studies, contributing to regulatory submissions, and driving innovation in methodologies and tools.

GSK

Hybrid Permanent

Director, Global Real-World Evidence & Health Outcomes Scientist, Oncology

This role involves planning, designing, and executing real-world evidence studies to support the commercial success and market positioning of GSK's oncology products. The Director will collaborate with internal and external stakeholders to ensure the generation of high-quality, scientifically credible evidence that meets regulatory and payer requirements.

GSK

On-site Permanent

Director, Global Real-World Evidence & Health Outcomes Scientist, Oncology

This role involves planning and executing real-world evidence studies to support the commercial success of GSK's oncology products. The Director will work closely with medical and commercial teams to ensure that evidence is aligned with regulatory and payer requirements, and will be responsible for managing timelines, budgets, and deliverables.

GSK

On-site Permanent

Director, Global Real-World Evidence & Health Outcomes Scientist, Oncology

This role involves planning and executing real-world evidence studies to support the launch and market positioning of GSK's oncology products. The Director will work closely with medical and commercial teams to ensure the generation of high-quality evidence that meets regulatory and payer requirements, driving successful patient access and commercial outcomes.

GSK

On-site Permanent

Director, Global Real-World Evidence & Health Outcomes Scientist, Oncology

This role involves planning and executing real-world evidence studies to support the launch and commercial success of GSK's oncology products. The Director will collaborate with internal and external stakeholders to ensure the generation of high-quality, scientifically credible evidence that meets regulatory and market requirements.

GSK

On-site Permanent

Medical Lead - Respiratory

This role involves leading the medical strategy for GSK's specialty respiratory portfolio, ensuring patient needs are at the forefront. Responsibilities include managing a medical therapy team, developing strategic plans, and engaging with healthcare professionals and regulatory bodies.

GSK United Kingdom

Hybrid Permanent

ViiV Healthcare (GSK) Clinical Development Manager

The Clinical Development Manager at ViiV Healthcare provides scientific leadership and direction for clinical development programs, focusing on the design and execution of high-quality studies. This role involves collaborating with cross-functional teams to ensure study protocols meet strategic objectives, overseeing data collection and analysis, and contributing to regulatory reporting and scientific outputs.

GSK United States

On-site Permanent

ViiV Healthcare (GSK) Clinical Development Manager

The Clinical Development Manager at ViiV Healthcare is responsible for providing scientific leadership and direction in the design and development of high-quality clinical studies. This role involves collaborating with cross-functional teams to ensure the accuracy and timeliness of study results, contributing to regulatory reporting, and creating scientific outputs for publications and presentations.

GSK

On-site Permanent

Study Manager

The Study Manager role involves leading and coordinating clinical and evidence generation studies, working with internal and external teams to ensure studies are on time, on budget, and compliant with standards. Key responsibilities include monitoring study progress, drafting clinical documents, coordinating meetings, and managing study communications and supplies.

GSK Stevenage, United Kingdom

Hybrid Permanent