Latest Clinical Research Associate Jobs

Senior Research Associate, Bioanalytical & Molecular Assays

This role involves developing, qualifying, and validating molecular bioanalytical assays—such as qPCR, ddPCR, and RT-qPCR—to support clinical pharmacokinetic and pharmacodynamic studies within a GCLp-compliant environment. The scientist will work closely with cross-functional teams to ensure robust data generation, maintain regulatory compliance, and integrate emerging digital and automation technologies into workflows. A strong focus on reagent management, assay documentation, and continuous process improvement is central to the position.

Moderna Oxford, United Kingdom

Hybrid Permanent

Senior Research Associate, Bioanalytical & Molecular Assays

This role involves developing, optimizing, and validating molecular bioanalytical assays—such as qPCR, ddPCR, and RNA isolation—to support mRNA-based clinical programs. The scientist will work within GCL0-compliant (GCLP) frameworks to generate pharmacokinetic and pharmacodynamic data, ensuring regulatory compliance and data integrity. Collaboration with cross-functional teams and adoption of digital tools and automation are key to advancing clinical trial execution and analytical processes.

Moderna

Hybrid Permanent

Associate Director of Clinical Sciences

This role involves leading clinical sciences activities within global oncology R&D, focusing on study design, protocol development, and clinical data review across the development lifecycle. The individual will act as a subject matter expert, ensuring scientific rigor and regulatory compliance while collaborating with cross-functional teams and external partners. A key focus is on immuno-oncology, with responsibilities spanning from early-phase to late-stage clinical development.

GSK

Clinical Development Director - Renal

The Clinical Development Director leads and supports clinical development activities within a global program, focusing on strategy, trial execution, data analysis, and regulatory documentation. This role involves close collaboration with cross-functional teams, ensuring scientific rigor and data quality across phases I–IV trials, particularly in late-phase development. The position requires strong scientific expertise, leadership in clinical operations, and active participation in safety and regulatory initiatives.

Novartis London, United Kingdom

Hybrid Permanent

Clinical Development Medical Director- Hepatology

Lead clinical development for hepatology assets, designing and executing translational and clinical studies to advance novel liver disease treatments. Provide medical oversight, shape development strategies, and collaborate across functions to deliver innovative medicines. Engage with regulators and external experts to drive proof-of-concept and lifecycle expansion opportunities.

GSK Stevenage, United Kingdom US$202,500 – US$371,250 pa

Hybrid Permanent

Clinical Development Medical Director - Neuromuscular

Leads global clinical development programs in neuroscience, with a focus on neuromuscular or related disorders. Provides medical leadership across trial design, regulatory submissions, and safety monitoring, collaborating with cross-functional teams and external stakeholders. Plays a strategic role in advancing innovative therapies through clinical execution and scientific insight.

Novartis London, United Kingdom £83,510 – £155,090 pa

Hybrid Permanent

Global Development Lead, Internal Medicine, Sr. Director (non-MD)

This role involves leading clinical development for internal medicine assets within Pfizer's Research & Development division, with a focus on obesity-related therapeutics. The Global Development Lead serves as the primary clinical accountability point, designing and executing global clinical development plans, regulatory submissions, and cross-functional team leadership. The position requires deep expertise in endocrinology or chronic weight management and extensive experience in Phase 1-3 clinical trials, translational medicine, and regulatory strategy across global markets.

Pfizer United States £214,900 – £358,100 pa

On-site Permanent

Global Development Lead, Internal Medicine, Sr. Director (non-MD)

This role leads clinical development for assigned assets in Internal Medicine within Pfizer's R&D division, with accountability for designing and executing global clinical development plans. The individual will guide cross-functional teams through trial design, regulatory submissions, and lifecycle management, while serving as a therapeutic expert and strategic partner across internal and external stakeholders. Emphasis is placed on innovation, patient engagement, and compliance with global regulatory standards.

Pfizer £214,900 – £358,100 pa

On-site Permanent

Associate Director, Safety Epidemiology – Global Patient Safety

Lead the design and execution of post-authorisation safety studies using real-world data to assess and communicate the safety profiles of AstraZeneca’s medicines. Provide strategic epidemiological input to regulatory submissions, safety signal evaluations, and diversity initiatives, collaborating with internal teams and external partners. Drive methodological excellence in pharmacoepidemiology and contribute to global patient safety decision-making across a broad product portfolio.

AstraZeneca Chatham, ME4 4NP, 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

Head, PV and Regulatory QA

Leads global pharmacovigilance and regulatory quality assurance, ensuring compliance with GVP, ICH, and regulatory standards across clinical safety, medical affairs, and regulatory affairs. Designs audit strategies, manages inspections, and oversees deviation management, CAPA, and change control systems. Provides cross-functional GxP expertise and drives continuous improvement in PV quality systems.

CSL

Director, CMC Regulatory Affairs

Lead CMC regulatory strategy for small molecule drugs in global clinical trials and marketing applications, overseeing high-quality submissions and advising on US, EU, and international regulations. Collaborate with cross-functional teams to interpret guidance, manage risks, and support clinical trial materials. Play a key role in shaping regulatory pathways within an AI-driven drug discovery environment.

Recursion North Tyneside, NE29 8EP, United Kingdom £207,500 – £280,720 pa

Remote Permanent

Director, CMC Regulatory Affairs

Lead the development and execution of CMC regulatory strategies for small molecule drugs in global clinical trials and marketing applications. Author and manage high-quality submissions including INDs, NDAs, and IMPDs across US, EU, and ROW regions. Provide strategic guidance on regulatory requirements, support clinical trial materials, and ensure compliance with evolving GMP standards.

Recursion London, W1C 2QP, United Kingdom £111,100 – £141,800 pa

Remote Permanent

Legal Counsel - Pharma/Life Sciences (12-month

Your new companyA global pharmaceutical and life sciences organisation is seeking an experienced Legal Counsel to join its UK & Ireland legal team on a 12-month contract. Operating at the forefront of healthcare innovation, the business develops and delivers medicines,...

Hays Legal Welwyn Garden City, Hertfordshire, AL8 6TP, United Kingdom £450 – £580 pd

Contract

Clinical Evaluation Specialist

This role involves conducting clinical evaluations with a focus on radiology and medical imaging technologies such as CT, PET, and fluoroscopy. The specialist will leverage clinical research experience, including participation in trials and publication of research papers, to support regulatory and consultancy projects. The position is based in London with a hybrid working arrangement.

Computer Futures London, City And County Of the City Of London, United Kingdom £75,000 – £90,000 pa

Hybrid Permanent