Latest Research Associate Jobs

Sr. Research Associate, Bioanalytical & Molecular Assays - Ligand Binding Assays

This role involves developing, optimizing, and validating ligand-binding and cell-based assays to support mRNA medicine development. The candidate will generate pharmacodynamic and immunogenicity data in compliance with GcLP, using platforms like Watson LIMS and electronic lab notebooks. They will also contribute to reagent management, assay documentation, and cross-functional collaboration with clinical teams to ensure robust, regulatory-compliant data delivery.

Moderna Oxford, United Kingdom

Hybrid Permanent

Sr. Research Associate, Bioanalytical & Molecular Assays - Ligand Binding Assays

This role involves developing, optimizing, and validating ligand-binding and cell-based assays to support mRNA medicine development. The candidate will generate pharmacodynamic and immunogenicity data from clinical samples in compliance with GcLP standards, using platforms like Watson LIMS and electronic lab notebooks. The position emphasizes regulatory compliance, critical reagent management, and collaboration with cross-functional teams to deliver high-quality bioanalytical data for clinical programs.

Moderna

Hybrid Permanent

Associate Director, Medical Affairs

This role involves shaping and executing medical strategy for immunology products across their post-launch lifecycle, with a focus on scientific engagement, evidence generation, and collaboration with key opinion leaders and internal teams. The position supports global medical and scientific communication, contributes to clinical understanding, and aligns with commercial and research partners. Based in Maidenhead or Zurich, it operates in a hybrid model with three days onsite weekly.

CSL

Hybrid Permanent

Associate Director, Regulatory Affairs

This role involves leading the development of global regulatory strategies for drug development programs, managing regulatory activities, and collaborating with cross-functional teams. The position requires extensive experience in regulatory affairs, with a focus on global health authorities and regulatory submissions.

Recursion North Tyneside, NE29 8EP, United Kingdom

On-site Permanent

Associate Director, Operations Excellence Supported Studies

This role focuses on strengthening the operational and digital foundations of GSK's Supported Studies, ensuring data integrity, system performance, and compliance. The individual will lead data governance, dashboard development, and system integration—particularly for platforms like Veeva and IdeaPoint—while acting as a bridge between business and technology teams to drive efficiency and compliance in clinical study delivery.

GSK London, United Kingdom US$154,275 – US$257,125 pa

Hybrid Permanent

Associate Director, Operations Excellence Supported Studies

This role focuses on strengthening the operational and data foundations for Supported Studies at GSK, ensuring data integrity, system performance, and compliance. The Associate Director will lead digital integration, dashboard governance, and process improvements, acting as a bridge between business and technology teams to enhance efficiency and regulatory adherence in clinical operations.

GSK United States US$154,275 – US$257,125 pa

Hybrid Permanent

Clinical Development Medical Director (Associate Director)

This role involves overseeing the medical and scientific aspects of clinical trials in Internal Medicine, ensuring data integrity and quality. Responsibilities include medical monitoring, safety data review, protocol development, and providing clinical support to the study team and external stakeholders.

Pfizer

On-site Permanent

Clinical Development Medical Director (Associate Director)

This role involves overseeing medical and scientific aspects of clinical trials in Internal Medicine, ensuring data integrity and quality. Responsibilities include medical monitoring, safety data review, protocol development, and collaboration with internal and external stakeholders.

Pfizer

On-site Permanent

Senior Clinical Development Medical Director - Renal

The Senior Clinical Development Medical Director will lead the strategy and execution of renal clinical development programs, from early to late phases. Responsibilities include providing clinical leadership, developing regulatory documents, ensuring patient safety, and collaborating with global teams and stakeholders.

Novartis

On-site Permanent

Senior Director, Project Operating Model and Leadership Excellence

This position will lead the transformation of project leadership capabilities across the R&D enterprise. On a systemic level, this role will prepare critical GPL roles (Exec Directors) to be CEO of the project via a bespoke leadership/drug development/executive training and...

CSL

Clinical Scientific Expert (CSE) I

Salary Range:£37,593.50 - £69,816.50Job Description SummaryWork Arrangement: Hybrid Working, #LI-HybridLocation: London (The Westworks), United KingdomRelocation Support: This role is based in London, United Kingdom. Novartis is unable to offer relocation support: please only apply if accessible.ABOUT THE ROLEThe Clinical Scientific...

Novartis London, United Kingdom

Principal Clinical Project Manager

This role leads complex or pivotal clinical trials from conception to closeout, overseeing cross-functional teams and vendor partnerships. The Principal Clinical Project Manager ensures study delivery within quality, timeline, and budget targets, applying risk-based quality management and driving inspection readiness. They also mentor junior staff and contribute to process improvements within clinical operations.

Autolus London, W12 7RH, United Kingdom

Hybrid Permanent

Senior Specialist I, QA Clinical

The Senior Specialist I, QA Clinical is responsible for quality oversight in clinical development, supporting cross-functional relationships and ensuring compliance with GCP/GVP regulations. Key responsibilities include developing and implementing risk-based audit plans, conducting audits, and managing quality events. The role involves working closely with clinical project teams and external stakeholders, and maintaining the quality management system.

Autolus Stevenage, United Kingdom

Hybrid Permanent Flexible

Talent Partner (Tech), London

As a Talent Partner at Isomorphic Labs, you will play a critical role in building world-class teams by developing and executing talent acquisition strategies. You will partner with senior leaders to attract top-tier talent, shape the company's future, foster an inclusive culture, and enhance the employer brand in the competitive AI and biotech landscape.

Isomorphic Labs London, United Kingdom

On-site Permanent

Senior Alliance Manager, London

This role involves managing and nurturing strategic scientific and business partnerships in a cutting-edge AI-driven drug discovery environment. The Senior Alliance Manager will oversee alliance governance, align internal and external teams, and ensure successful delivery of collaborative research and development programs. The position plays a key role in scaling operational frameworks and fostering a collaborative culture across high-impact partnerships.

Isomorphic Labs London, United Kingdom

Hybrid Permanent