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

Clinical Data Strategy, Manager

This role involves leading clinical data strategy planning and execution across Translational Medicine programs, with a focus on designing fit-for-purpose data collection approaches and supporting robust decision-making. The individual will develop Data Strategy Plans, guide trial teams on data oversight, and leverage internal and external data to inform trial design—particularly in Neuroscience. The position requires deep expertise in clinical assessments, data integrity, and cross-functional collaboration in a global, fast-paced environment.

Novartis London, United Kingdom £49,140 – £91,260 pa

Hybrid Permanent

*Senior Clinical Development Medical Director - Renal

Leads the end-to-end clinical development strategy for renal programs, from early through registrational phases. Provides medical leadership across trial design, regulatory documentation, and safety oversight. Works cross-functionally to translate data into clinical and regulatory pathways, ensuring robust benefit-risk decision-making throughout the program lifecycle.

Novartis London, United Kingdom

On-site 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- Hepatology

Lead clinical development strategy and execution for hepatology programs, designing and overseeing translational and clinical studies to advance novel liver disease treatments. Provide medical leadership across cross-functional teams, contribute to regulatory interactions, and drive innovation in drug development. Focus on identifying high-impact targets and delivering differentiated medicines with strong scientific and clinical foundations.

GSK £202,500 – £371,250 pa

Hybrid Permanent

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

Leads clinical development for assigned assets in Internal Medicine, serving as the primary clinical accountability point within Pfizer's Research & Development. Designs and oversees global clinical trials, regulatory submissions, and cross-functional team coordination, with potential involvement in obesity-related late-stage programs. Engages with external stakeholders and ensures compliance with scientific, regulatory, and safety standards.

Pfizer England

On-site 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 therapies. The Global Development Lead will design and oversee global clinical trials, create development plans, and ensure regulatory compliance across regions including China and Japan. The position requires cross-functional leadership, engagement with external stakeholders, and contribution to regulatory submissions and product labeling.

Pfizer England £214,900 – £358,100 pa

On-site Permanent

Associate Director Audit & Assurance R&D Q&A

This role involves leading risk-based GVP and GCP audit programs within AstraZeneca’s R&D quality assurance function, ensuring compliance across clinical and research operations. The individual will drive inspection readiness, manage critical CAPAs, and provide expert GxP guidance across emerging fields like AI, digital health, and cell therapy. They will also shape quality systems, mentor teams, and support due diligence, directly influencing patient safety and regulatory success.

AstraZeneca Chatham, ME4 4NP, United Kingdom

Hybrid Permanent

Associate Director, Systems Medicine

This role involves developing and applying mechanistic systems pharmacology and toxicology (QSP/T) models to inform dose selection and clinical strategy across drug development phases. The individual will lead compound-specific modelling projects, integrate data from microphysiological systems, and use virtual populations to predict efficacy and safety. Collaboration with cross-functional teams and mentorship of junior modelers are key aspects of the position.

AstraZeneca Cambridge, United Kingdom

Hybrid Permanent

Bank Biomedical Scientist

Bank Biomedical Scientist/Spire Manchester / 0 HoursSpire Manchester Hospital has an exciting opportunity for a Biomedical Scientist to join the team on a Bank 0-hour contract.Duties and responsibilities:To assist in the organisation, management and development of services within specialty of...

Spire Healthcare Manchester, United Kingdom

Senior Biomedical Scientist Training Lead

Senior Biomedical Scientist Training Lead | Pathology | Full Time | Permanent | ManchesterJob PurposeTo assist in the organisation, management and development of services within a specialised area of the pathology service, or across a range of services provided by...

Spire Healthcare Manchester, United Kingdom

Head, PV and Regulatory QA

This role leads the global quality and compliance function for pharmacovigilance (PV) systems, ensuring adherence to international regulations and internal standards across clinical safety, regulatory affairs, and medical affairs. The position combines strategic oversight with hands-on operational leadership, including audit strategy, inspection readiness, deviation and CAPA management, and cross-functional GxP guidance. It requires deep technical expertise in PV processes and strong leadership to drive quality across global teams and third-party vendors.

CSL

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

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