Latest Clinical Research Associate Jobs

Clinical Research Associate

This role involves managing and monitoring clinical trial sites remotely, ensuring compliance with Good Clinical Practice and Pfizer standards. The Clinical Research Associate serves as the primary point of contact for investigator sites, conducting remote and on-site monitoring, supporting patient safety, resolving protocol issues, and driving site activation and recruitment. The position emphasizes strong collaboration with study teams and site staff to maintain data quality and regulatory compliance throughout the trial lifecycle.

Pfizer United Kingdom

Remote Permanent

Senior Clinical Research Associate I

This role involves managing and monitoring clinical trial sites to ensure compliance with protocols, patient safety, and data quality. The Senior Clinical Research Associate I serves as the primary point of contact for investigator sites, conducts on-site and remote monitoring, supports enrollment, resolves protocol issues, and ensures adherence to Good Clinical Practice and regulatory standards. The position requires close collaboration with study teams and site staff within a flexible, remote-working environment.

Pfizer United Kingdom

Remote Permanent

Clinical Study Administrator

As a Clinical Study Administrator, you will coordinate and manage the administrative aspects of clinical trials, ensuring that all documentation, regulatory submissions, and stakeholder communications are accurate and timely. You will work closely with various teams to maintain inspection readiness and support the smooth operation of multi-site studies.

AstraZeneca Chatham, ME4 4NP, United Kingdom

On-site Permanent

Executive Medical Director

Work with usOur team are passionate in the pursuit of excellence and in pushing the boundaries of cancer therapy and Autoimmune disease to deliver life-changing treatments to patients.Whilst working at Autolus you will enjoy a flexible, diverse and dynamic working...

Autolus London, W12 7RH, United Kingdom

Hybrid Permanent

Principal Research Associate, Clinical Biomarker Laboratory, Flow Cytometry

This role involves leading high-parameter spectral flow cytometry activities in a GCLP-compliant clinical laboratory, generating immunophenotyping and functional immune profiling data from PBMC and whole blood samples to support mRNA-based clinical development. The scientist will independently execute and analyze complex assays, contribute to assay development and validation, and ensure regulatory compliance while leveraging advanced platforms like the Cytek Aurora. Opportunities exist to engage with digital tools and generative AI for data interpretation and workflow optimization within a collaborative, innovation-driven environment.

Moderna Oxford, United Kingdom

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 conduct experiments, analyze data, and ensure regulatory compliance in a GCP environment, contributing directly to patient-impacting therapeutics across multiple disease areas.

Moderna Oxford, United Kingdom

Hybrid Permanent

Research Associate, Compound Management

The Research Associate will manage inventory, prepare reagents, and run automated systems for high-throughput screening. They will collaborate with cross-functional teams to optimize workflows and adopt new technologies, contributing to the company's drug discovery platform.

Recursion United Kingdom

On-site Permanent

Research Associate, Assay Operations (Contractor)

This role involves executing high-throughput, multi-omics screening experiments using automated lab systems in 384- and 1536-well plates to generate data for drug discovery. The candidate will prioritize production workflows, maintain equipment and reagents, and contribute to process improvements through automation and optimization. Collaboration, proactive communication, and adherence to SOPs are essential in this fast-paced, mission-driven environment.

Recursion United Kingdom

On-site Contract

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 London, United Kingdom

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

SERM Associate Medical Director

This role involves providing medical and scientific expertise in safety evaluation and risk management for GSK's clinical and post-marketing assets. Responsibilities include signal detection, data analysis, and communication of safety risks, as well as supporting safety governance and cross-functional teams.

GSK United Kingdom

Hybrid Permanent

Associate Director, Biostatistics (2)

The Associate Director, Biostatistics, leads the statistical contribution to clinical development programs, ensuring appropriate methodologies for study design, data analysis, and regulatory submissions. They collaborate with cross-functional teams, manage outsourcing operations, and represent Biostatistics in regulatory interactions.

CSL United Kingdom

On-site Permanent

Associate Director, Biostatistics (2)

The Associate Director, Biostatistics, leads the statistical contribution to clinical development programs, defining statistical strategies, ensuring appropriate methodologies, and collaborating with cross-functional teams. They also manage outsourcing operations, represent Biostatistics in regulatory interactions, and support innovation in clinical trial design and analysis.

CSL

On-site 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 capability and quality.

GSK Stevenage, United Kingdom

Hybrid Permanent

Associate Director, Biostatistics 2

The role involves leading the statistical aspects of clinical development programs, including study design, data analysis, and regulatory submissions. Responsibilities include collaborating with cross-functional teams, managing CROs, and representing Biostatistics in regulatory interactions.

Appcast Enterprise Maidenhead, SL6 1QB, United Kingdom

On-site Permanent