Latest Clinical Research Associate Jobs

Medical Director, Oncology Clinical Development - Hematology

The Medical Director, Oncology Clinical Development - Hematology is a physician-led role focused on guiding clinical strategy and medical oversight in oncology drug development. This position involves leading medical monitoring, interpreting clinical and safety data, contributing to protocol design, and engaging with investigators and regulatory bodies. The role operates within cross-functional teams to ensure patient safety and clinical integrity across Phase I–III trials in hematology and oncology.

GSK United States

Medical Director, Oncology Clinical Development - Hematology

This role involves leading medical oversight in oncology clinical development, focusing on hematology. The Medical Director will guide study design, ensure patient safety, interpret clinical data, and collaborate with cross-functional teams and external experts. It emphasizes physician leadership in trials from Phase I–III, with a strong focus on real-world impact and regulatory engagement.

GSK £222,750 – £371,250 pa

Associate Director, Computational Biology – Early Discovery

Lead a team of computational biologists to identify and validate novel oncology targets using integrated phenomics, transcriptomics, genomics, and proteomics data. Develop and scale methods for target discovery in oncology and immunological diseases, collaborating closely with biologists, data scientists, and engineers. Drive data strategy and present findings to stakeholders to advance drug discovery programs.

Recursion United Kingdom

On-site Permanent

Don't see what you're looking for?

This is a general talent network sign-up opportunity rather than a specific job role. Candidates can submit their resume for future consideration at Recursion, a clinical-stage TechBio company using AI and automated biology to accelerate drug discovery. The company emphasizes bold, ethical innovation and cross-functional collaboration to address unmet medical needs.

Recursion United Kingdom

On-site Permanent

Associate Director, Regulatory Diagnostics

Designs and leads global regulatory strategies for precision diagnostics, including companion diagnostics and in vitro devices, integrated within drug development programs. Works cross-functionally to manage submissions, health authority interactions, and compliance across lifecycle stages in a collaborative, innovation-driven environment.

Novartis London, United Kingdom £67,900 – £126,100 pa

Hybrid Permanent

Global Labelling Associate Director, Content (Oncology)

This role involves leading the development and maintenance of global labelling strategies and core documents for oncology products, ensuring scientific accuracy and regulatory compliance. The individual will facilitate cross-functional alignment, analyse regulatory and competitor data, and support health authority interactions. Based remotely or in London, the position plays a key part in shaping product information across global markets.

Novartis

Hybrid Permanent

Senior Director, Translational Genetics

Leads a team of translational genetics scientists to integrate genetic, genomic (especially proteomics), and clinical data in support of drug discovery and development. Focuses on addressing key translational questions across therapeutic areas such as respiratory, hepatology, neurodegeneration, and immunology. Works within cross-functional teams and drives external scientific collaborations to advance GSK’s R&D pipeline.

GSK US$207,075 – US$345,125 pa

Hybrid Permanent

Senior Director, Structured Component Management (SCM) Strategy, Operations & Governance

Lead the design and governance of structured component management standards across R&D, ensuring compliance with regulatory and GxP requirements. Drive adoption of component-based authoring, metadata frameworks, and lifecycle governance, with a focus on audit readiness and scalability for AI-assisted content generation. Partner with cross-functional teams to build training, ensure compliance, and evolve standards in a global, regulated environment.

GSK Stevenage, United Kingdom

Hybrid Permanent

Sr Director and Team Lead, Regulatory Labelling Strategy and Development, Oncology

Leads a global team responsible for developing and managing regulatory labelling strategies for oncology products across the drug development lifecycle. Ensures compliance with global regulations, collaborates with cross-functional stakeholders in R&D, safety, and commercial teams, and engages with regulatory authorities to shape innovative, patient-focused labelling. Plays a strategic role in governance and policy development within GSK’s oncology portfolio.

GSK £221,925 – £369,875 pa

Senior Director, Structured Component Management (SCM) Strategy, Operations & Governance

Lead the design and governance of structured component management standards across R&D, ensuring compliance with regulatory requirements and enabling AI-assisted authoring workflows. Drive adoption of component taxonomies, metadata schemas, and lifecycle frameworks while operating a component registry and supporting audit readiness. Partner with cross-functional teams to build capabilities and evolve standards in a global, regulated environment.

GSK

Hybrid Permanent

Senior Director, Structured Component Management (SCM) Strategy, Operations & Governance

Leads the design and governance of structured component management standards across R&D, ensuring compliance with regulatory requirements and enabling AI-assisted authoring workflows. Oversees component taxonomy, metadata schemas, lifecycle governance, and audit readiness. Works cross-functionally with medical writing, regulatory, quality, and data governance teams to drive adoption and maintain standards.

GSK

Hybrid Permanent

Senior Director, Structured Component Management (SCM) Strategy, Operations & Governance

Lead the design and governance of structured component management standards across R&D, ensuring compliance with regulatory requirements and enabling AI-assisted authoring workflows. Drive adoption of component taxonomy, metadata schemas, and lifecycle governance while collaborating with cross-functional teams in a regulated pharmaceutical environment.

GSK

Hybrid Permanent