Latest Clinical Research Associate Jobs

Senior Clinical Research Associate II

This role involves managing and monitoring clinical trial sites to ensure compliance with Good Clinical Practice and Pfizer standards, with a focus on patient safety and data quality. The Senior Clinical Research Associate acts as the primary point of contact for investigator sites, supporting study setup, execution, and closeout while addressing protocol issues and driving recruitment. The position requires extensive interaction with site staff, cross-functional teams, and vendors, using both on-site and remote monitoring methods.

Pfizer United Kingdom

Remote Permanent

Principal Research Associate, Clinical Biomarker Laboratory, Flow Cytometry

This role involves generating and analyzing high-parameter flow cytometry data from clinical trial samples to support immunology research in a GCLP-compliant environment. The scientist will operate advanced spectral flow platforms like the Cytek Aurora, perform ex vivo immune functional assays, and ensure data integrity through rigorous documentation and compliance. Emphasis is placed on innovation through AI-enabled tools, assay development, and mentoring within a collaborative, regulated laboratory setting.

Moderna

Hybrid Permanent

Senior Research Associate, Clinical Biomarker Laboratory, Immunoassays

This role involves hands-on development, qualification, and validation of functional immunoassays to support mRNA-based clinical trials. The scientist will generate and analyze high-quality data in a GCP-compliant lab environment, contribute to assay innovation, and ensure regulatory compliance. Collaboration with cross-functional teams and use of digital tools, including AI-enabled platforms, are integral to supporting clinical development objectives.

Moderna

On-site Permanent

Research Associate, Primary Pharmacology

This role involves developing and optimizing cell-based and biochemical assays to support small molecule drug discovery, with a focus on compound characterization and candidate identification. The scientist will work in a high-throughput, automated lab environment, generating decision-ready data in collaboration with cross-functional teams. The position emphasizes hands-on experimentation, assay innovation, and integration within a multidisciplinary drug discovery pipeline.

Recursion Crathes, Alba / Scotland, United Kingdom £41,000 – £52,000 pa

On-site Permanent

Research Associate - Biology Automation

This role involves developing and running automated biochemical and cell-based assays to support drug discovery projects. You will work on a leading-edge automation platform, ensuring high-quality data and collaborating with cross-functional teams to drive small molecule therapeutics development.

Recursion Crathes, Alba / Scotland, United Kingdom

On-site Permanent

Clinical Development Medical Director (Associate Director)

This role involves overseeing medical and scientific aspects of clinical trials in Internal Medicine, including medical monitoring, safety data review, and clinical data management. The Medical Director will also contribute to protocol design, site selection, and investigator training, while mentoring others and ensuring data integrity and quality.

Pfizer Manchester, M1 4HD, United Kingdom

On-site Permanent

Associate Director, Biostatistics (4)

The Associate Director (AD), Biostatistics, leads the full scope of statistical contribution to a clinicaldevelopment program. The AD provides statistical strategies for the clinical trials and regulatorysubmissions, and is accountable for the statistical deliverables within the program.Lead full scope of...

CSL

Associate Director, Biostatistics (4)

The Associate Director (AD), Biostatistics, leads the full scope of statistical contribution to a clinicaldevelopment program. The AD provides statistical strategies for the clinical trials and regulatorysubmissions, and is accountable for the statistical deliverables within the program.Lead full scope of...

CSL

Statistics Leader / Associate Director – Oncology Statistics

This role involves leading statistical planning and delivery for clinical programs in oncology, working closely with cross-functional teams to design robust clinical trials and contribute to regulatory strategy. The position also focuses on methodological innovation and mentoring colleagues to build statistical capability and quality.

GSK United Kingdom

Hybrid Permanent

Statistics Leader / Associate Director – Oncology Statistics

This role involves leading statistical planning and delivery for clinical programs in oncology, working closely with cross-functional teams to design robust clinical trials and contribute to regulatory strategies. The position also focuses on methodological innovation and mentoring colleagues to build statistical capabilities.

GSK

Hybrid Permanent

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

Clinical Development Director - Renal

The Clinical Development Director is responsible for leading and supporting the delivery of clinical deliverables for a section of a global clinical program or a large, complex trial. This role involves collaborating with various teams to ensure data quality, regulatory compliance, and scientific accuracy in clinical trials and publications.

Novartis London, United Kingdom

Hybrid Permanent

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

Associate Director, Systems Medicine

This role involves developing and applying mechanistic systems models in pharmacology and toxicology to inform dose and schedule decisions across clinical development. The candidate will lead quantitative systems pharmacology (QSP) and toxicology (QST) modelling efforts, integrate data from organ-on-chips and organoids, and collaborate with multidisciplinary teams to translate scientific insights into patient impact. The position emphasizes innovation in virtual populations, digital twin approaches, and decision-making influence across therapy areas.

AstraZeneca Cambridge, United Kingdom

Hybrid Permanent

Associate Director, Safety Epidemiology – Global Patient Safety

This role involves leading the design, execution, and reporting of post-authorisation safety studies using real-world data. The candidate will collaborate with various teams to produce high-quality evidence for regulatory decisions and risk management, ensuring AstraZeneca's medicines are safe and effective.

AstraZeneca Chatham, ME4 4NP, United Kingdom

On-site Permanent