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

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 Operations Specialist (Contracts)

This role involves leading the coordination and lifecycle management of clinical trial contracts and legal documents in compliance with ICH GCP, UK regulations, and GSK standards. The specialist will negotiate investigator and supplier contracts, manage budget development, ensure TMF completeness, and act as a point of contact for legal and contracting issues. The position supports clinical operations through digital tools, including AI-enabled solutions and CLM platforms, while providing training and administrative support to local and global teams.

GSK United Kingdom

Senior Clinical Development Medical Director

This role involves leading clinical strategy and execution for cardiovascular/stroke medicine programs, with responsibility for trial design, regulatory documentation, and cross-functional collaboration. The Senior Clinical Development Medical Director will guide global teams, interpret complex clinical data, and contribute to safety and development decisions across the drug lifecycle. Expertise in anticoagulation and outcome trials is key, along with strong leadership in a matrix environment.

Novartis London, United Kingdom

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

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

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

Global Clinical Head, Respiratory

Lead clinical strategy and scientific oversight for a respiratory product within a global pharmaceutical team, driving late-phase clinical development, regulatory submissions, and benefit/risk assessments. Responsible for cross-functional leadership, mentoring clinical teams, and aligning clinical components of the Target Product Profile and development plans. Engages with regulatory agencies and commercial stakeholders to shape global scientific and medical direction.

AstraZeneca Cambridge, United Kingdom

Senior Medical Director Early Clinical Respiratory

This role involves leading early-phase clinical development in respiratory therapeutics, designing and overseeing Phase 1 and 2a trials, and translating scientific innovation into clinical proof-of-concept. The individual will act as a medical expert, shaping clinical strategies, guiding regulatory interactions, and mentoring teams within a global, collaborative environment. Emphasis is placed on biomarker use, translational research, and engagement with external scientific leaders.

AstraZeneca Cambridge, United Kingdom

Junior Technical Specialist (Microbiology & Immunology)

Performs and oversees microbiology and immunology assays including bacterial culture, flow cytometry, ELISA, and functional immune testing to support vaccine research. Ensures high-quality, compliant laboratory operations within a regulated environment. Contributes to assay optimisation and troubleshooting in collaboration with senior scientists.

University of Oxford Oxford, South East England, United Kingdom £35 – £41 pa

Contract

Applied Research Engineer - Post-Training

This role involves owning the full post-training lifecycle of biological foundation models, designing pipelines to adapt them for specific drug discovery applications, and validating performance against biological data. The engineer will work directly on therapeutic use cases, making core technical decisions and delivering models that inform real clinical programs. Close collaboration with ML infrastructure and biology teams ensures scientific validity and production readiness.

Helical London, United Kingdom

On-site Permanent