Latest Research Associate Jobs

(Fixed Term) Senior Research Associate, Clinical Biomarker Laboratory, Flow Cytometry

This role involves working as a technical expert in the Clinical Flow Cytometry group at Moderna's Harwell facility, generating high-quality clinical trial data through advanced flow cytometry assays. Responsibilities include executing clinical sample testing, conducting immune profiling, and ensuring data integrity and compliance with GCLP standards.

Moderna Oxford, United Kingdom

On-site Contract

(Fixed Term) Senior Research Associate, Clinical Biomarker Laboratory, Flow Cytometry

This role involves working as a technical expert in the Clinical Flow Cytometry group at Moderna's Harwell facility, focusing on generating high-quality clinical trial data through advanced flow cytometry assays. Responsibilities include executing clinical sample testing, conducting immune profiling, and ensuring data integrity and compliance with GCLP standards.

Moderna

On-site Contract

Associate Director, R&D Project Management

CSL is transforming its R&D organization to accelerate innovation and create greater impact for patients. With a streamlined, project-led structure and a focus on collaboration, we're building a future-ready team that excels in dynamic biotech ecosystems. Joining CSL now means...

CSL

Hybrid Permanent

Associate Director, Medical Affairs

This role involves shaping medical strategy for immunology products, supporting post-launch lifecycle management, and driving scientific engagement with key opinion leaders and patient groups. The individual will coordinate investigator-led studies, provide scientific input to commercial teams, and support evidence generation across global markets. Collaboration with cross-functional teams and affiliates is central to advancing clinical understanding and therapeutic impact.

CSL United Kingdom

Hybrid Permanent

Associate Director, CMC Regulatory Affairs

This role involves leading the development and implementation of CMC regulatory strategies for small molecule drugs in global clinical trials. Responsibilities include managing CMC submissions, providing regulatory guidance, and supporting cross-functional teams in navigating international regulations.

Recursion London, W1C 2QP, United Kingdom £88,200 – £111,100 pa

Hybrid Permanent Flexible

Associate Director, CMC Regulatory Affairs

This role involves leading the development and implementation of CMC regulatory strategies for small molecule drugs in global clinical trials. Responsibilities include managing CMC submissions, providing regulatory guidance, and collaborating with cross-functional teams to ensure compliance with US, EU, and ROW regulations.

Recursion United Kingdom £176,400 – £228,250 pa

Hybrid Permanent Flexible

Statistics Leader / Associate Director – Oncology Statistics

This role involves leading statistical planning and delivery for clinical programs in oncology, working closely with cross-functional teams to design robust clinical trials and contribute to regulatory strategy. The position also focuses on methodological innovation and mentoring colleagues to build statistical capability and quality.

GSK

Hybrid Permanent

Associate Director, Operations Excellence Supported Studies

This role leads operational excellence for Supported Studies at GSK, focusing on data governance, system ownership, and digital integration. The individual will ensure data integrity, drive compliance with regulatory requirements like Transfer of Value, and translate operational needs into scalable digital solutions. Working across cross-functional teams, they will enhance efficiency, quality, and transparency in clinical operations through robust dashboards, automation, and process improvements.

GSK Stevenage, United Kingdom US$154,275 – US$257,125 pa

Hybrid Permanent

Translational Medicine Expert – Dermatology, Associate Director

This role involves leading translational medicine strategies in dermatology, spanning early to late-stage drug development. The expert will drive clinical pharmacology, biomarker development, and regulatory strategies while collaborating across research, development, and external stakeholders. Key responsibilities include study design, safety oversight, and scientific leadership in global project teams.

Novartis London, United Kingdom £67,900 – £126,100 pa

Hybrid 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 collaboration with internal and external stakeholders.

Pfizer

On-site Permanent

Clinical Development Medical Director (Associate Director)

The Clinical Development Medical Director (Associate Director) oversees 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 clinical support for studies, with potential mentorship and strategic input.

Pfizer

On-site Permanent

Senior Clinical Development Medical Director - Renal

The Senior Clinical Development Medical Director will lead the strategy and execution of renal clinical development programs, from early to late phases. Responsibilities include providing clinical leadership, developing regulatory documents, ensuring patient safety, and collaborating with global teams and stakeholders.

Novartis London, United Kingdom

On-site Permanent

Senior QA Specialist, Pharmaceutical Development Quality Assurance (Maternity Leave Cover / Home Based)

This role involves ensuring the quality and compliance of Investigational Medicinal Products (IMPs) developed and manufactured by contract partners. The Senior QA Specialist will lead batch reviews, manage product stability programs, conduct vendor audits, and maintain quality systems in line with cGMP standards. The position supports clinical trial supply readiness and regulatory compliance across the pharmaceutical development lifecycle.

Jazz Pharmaceuticals London, United Kingdom

Remote Contract

PhD Level Ultrasound Technology Consultant - Cambridge

This role involves advancing surgical and interventional medical technologies through the application of deep ultrasound expertise. You'll lead high-impact technical programmes from feasibility to market readiness, working on intelligent instruments and robotic surgical systems. Collaboration with multidisciplinary teams and external partners is central, with a focus on solving complex scientific challenges and translating innovations into real-world clinical applications.

Newton Colmore Cambridge, Cambridgeshire, United Kingdom

On-site Permanent

Software Engineer

This role involves leading the development of Owkin’s Data Transformation Agent (DTA) and contributing to the core components of the platform. You will design and maintain complex data transformation workflows, manage deployments, and collaborate with internal stakeholders to ensure high standards in code and technical practices.

Owkin United Kingdom

Remote Permanent