Latest Clinical Research Associate (CRA) Jobs

Global Study Manager

The Global Study Manager role involves leading the operational delivery of clinical studies from initiation to archiving, ensuring timelines, quality, and budget adherence. Key responsibilities include crafting delivery plans, leading the Operational Working Group, and ensuring compliance with ICH/GCP guidelines. The role emphasizes innovation, risk management, and stakeholder communication.

GSK

Hybrid 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 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 study teams 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 providing clinical support to study teams and investigators.

Pfizer

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

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.1 Lead full scope...

CSL

Associate Director, Biostatistics

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.1 Lead full scope...

CSL

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

Biomedical Scientist

Biomedical Scientist | Pathology | Full Time | Perm | ManchesterWe're looking for a motivated Biomedical Scientist to join our Pathology team at Manchester Hospital. This full‑time, role offers the chance to work in a supportive, well‑equipped laboratory while playing...

Spire Healthcare Manchester, United Kingdom

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

Business Analyst

The Business Analyst will support a key programme focused on the collection, tracking, and lifecycle management of human biological samples. Responsibilities include eliciting and documenting requirements, mapping end-to-end processes, and facilitating stakeholder workshops to enhance biobanking systems and data flows.

DCV Technologies Stevenage, Hertfordshire, United Kingdom £400 – £450 pd

Hybrid Contract

Bioinformatics Engineer (we have office locations in Cambridge, Leeds & London)

The Bioinformatics Engineer will develop and scale knowledge platforms for the NHS Whole Genome Sequencing (WGS) Genomic Medicine Service, including PanelApp and CellBase. Responsibilities include building APIs, data models, and pipelines, collaborating with genomic data scientists, and ensuring clinical and biological accuracy in software. The role involves working in an agile team to deliver high-quality, clinically relevant genomic knowledge systems.

Genomics England Cambridge, Cambridgeshire, United Kingdom £56,000 – £65,000 pa

On-site Permanent Clearance Required

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

Radiopharmaceutical QP

CMDO is Seeking to Appoint a Qualified Person. The Organisation is Engaged in Developing and Manufacturing New Medicines and Novel Formulations, Including a Wide Range of Oral Solid and Liquid Dosage Forms, Sterilised and Aseptically Filled Products, as well as...

CV-Library City of Westminster, Greater London

Clinical Data Analyst – Evinova

The Clinical Data Analyst role involves managing and optimizing clinical trial data, collaborating with cross-functional teams, and contributing to the development of data products. Responsibilities include data management, standards validation, pipeline configuration, troubleshooting, and continuous process improvement.

AstraZeneca London, United Kingdom

On-site Permanent