Latest Clinical Research Associate Jobs

Principal Research Associate, Clinical Biomarker Laboratory, Flow Cytometry

This role involves generating and analyzing high-parameter flow cytometry data under GCLP guidelines to support clinical development in immunology. The scientist will perform immunophenotyping, functional immune profiling, and assay development using spectral flow platforms like Cytek Aurora, while ensuring data integrity and regulatory compliance. The position emphasizes technical expertise, collaboration, and the use of advanced data analysis tools including AI-enabled platforms.

Moderna Oxford, United Kingdom

Hybrid Permanent

Principal Research Associate, Clinical Biomarker Laboratory, Flow Cytometry

This role involves generating and analyzing high-parameter flow cytometry data from clinical trial samples in a GCLP-compliant laboratory environment. The Principal Research Associate will operate advanced spectral flow cytometers like the Cytek Aurora, perform PBMC isolation and functional immune assays, and support assay development and validation. Emphasis is placed on data integrity, regulatory compliance, and the use of digital tools including AI-enabled platforms for workflow optimization and data interpretation.

Moderna

Hybrid Permanent

Associate Director of Clinical Sciences

Lead clinical sciences strategy and execution for global oncology studies, with responsibility for end-to-end protocol development, clinical data review, and cross-functional collaboration. Focus on immuno-oncology with strong emphasis on regulatory compliance, patient safety, and scientific leadership across clinical development phases. Work within a matrix environment to guide study design, interpretation, and regulatory submissions.

GSK Stevenage, United Kingdom

Associate Director of Clinical Sciences

This role involves leading clinical sciences activities in global oncology studies, with responsibility for end-to-end protocol development, clinical data review, and cross-functional collaboration. The individual will shape study design, interpret results, and ensure regulatory compliance across phases of development, with a focus on immuno-oncology. The position requires scientific leadership, engagement with external experts, and contribution to regulatory submissions and clinical strategy.

GSK United States

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

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

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

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

Business Analytics, Forecasting & CI Associate

This role involves generating actionable commercial insights through competitive intelligence, market research, and forecasting to support Autolus' pipeline of T cell therapies. The associate will analyse market dynamics, monitor competitors, and synthesise data from multiple sources to inform strategic decision-making across commercial and clinical assets. It is a cross-functional position requiring coordination with external vendors and internal stakeholders to deliver evidence-based reports and dashboards.

Autolus London, W12 7RH, United Kingdom

Contract

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

Clinical Research Fellow in Biomedical Ultrasound for Wound Therapy

Act as the Key Local Investigator in a clinical research study focused on biomedical ultrasound for wound therapy, ensuring adherence to trial protocols and SOPs. Responsibilities include participant counselling and consent, maintaining medical records, supporting multidisciplinary clinics, and collaborating with senior researchers. Based at the Botnar Institute for Musculoskeletal Sciences within the University of Oxford.

University of Oxford Oxford, South East England, United Kingdom £38 – £52 pa

On-site Contract Part-time

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