Latest clinical research associate Jobs

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 clinical-stage mRNA programs in a GCL0-compliant environment. The scientist will generate high-quality PK/PD data, ensure regulatory compliance, and collaborate across functions to advance assays from research into clinical development. Emphasis is placed on data integrity, digital innovation, and integration of emerging technologies including automation and AI-enabled workflows.

Moderna Oxford, United Kingdom

Hybrid Permanent

Senior Research Associate, Bioanalytical & Molecular Assays

This role involves developing, qualifying, and validating molecular bioanalytical assays—such as qPCR, ddPCR, and gel electrophoresis—to support clinical-stage mRNA programs. The scientist will generate high-quality RNA quantitation data in compliance with GCLP standards, collaborate across clinical and laboratory teams, and contribute to regulatory documentation and sample management strategies. The position emphasizes innovation through digital tools and automation within a fast-paced, compliance-driven environment.

Moderna

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

Clinical Development Medical Director - Neuromuscular

This role involves leading clinical development programs in neuroscience, with a focus on neuromuscular or related disorders. The Medical Director will shape clinical strategy, oversee trial execution, interpret data, and engage with regulatory and external experts to advance innovative therapies. It requires strong medical and scientific leadership within a global, cross-functional environment.

Novartis Ardross, Alba / Scotland, IV17 0YF, United Kingdom £83,510 – £155,090 pa

Hybrid Permanent

Associate Director, Technology & Scientific Computing

Job Description SummaryWe are seeking a highly experienced Lead Business Analyst with strong pharmaceutical domain expertise and deep R programming capabilities to support a global pharmaceutical engagement.This role will act as the primary interface between business stakeholders, biostatisticians, statistical programmers,...

Novartis India

Medical Director - Oncology Clinical Development

The Medical Director will lead the development of oncology treatments, collaborating with a multidisciplinary team to design and execute clinical trials from early to late stages. Responsibilities include medical oversight, protocol development, safety monitoring, and strategic partnerships with key stakeholders.

GSK

Hybrid Permanent

Medical Director - Oncology Clinical Development

The Medical Director, Oncology Clinical Development, will lead the design and execution of clinical trials for GSK's oncology portfolio, focusing on hematological malignancies. Key responsibilities include collaborating with multidisciplinary teams, ensuring patient safety, and contributing to regulatory submissions and publications.

GSK Stevenage, United Kingdom

Hybrid Permanent

Head of Early Discovery

Your work will change lives. Including your own.The impact You'll MakeThe Head of Early Discovery will lead strategic initiatives to accelerate drug discovery by leveraging cutting-edge technologies, data-driven decision-making, and innovative scientific approaches. This role is pivotal in shaping Recursion’s...

Recursion United Kingdom

Director, Portfolio Development Process & Standards Lead

This role leads the establishment and maintenance of processes and standards across CSL's global Portfolio Development function, ensuring high-quality clinical trial planning, evaluation, and reporting. The Director will drive process improvement, SOP governance, training curriculum development, and cross-functional change initiatives within a dynamic biotech R&D environment. They will work closely with leadership and international teams to reduce complexity, improve quality and speed, and align procedural frameworks across clinical development, biomarkers, and commercial operations.

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, Regulatory Affairs

This role involves leading the development of global regulatory strategies for drug development programs, managing regulatory activities, and collaborating with cross-functional teams. The position requires extensive experience in regulatory affairs, with a focus on global health authorities and regulatory submissions.

Recursion North Tyneside, NE29 8EP, 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

Business Insights Manager or Secondment)

The Business Insights Manager will analyze data from various sources, including sales and market activity, to develop actionable recommendations that support AstraZeneca’s strategic goals. Key responsibilities include leading market research projects, forecasting, and collaborating with teams in Marketing, Finance, and Market Access, specifically focusing on the Cardio-Renal therapy area.

AstraZeneca London, United Kingdom

Hybrid Contract

Senior Alliance Manager, London

This role involves managing and nurturing strategic scientific and business partnerships in a cutting-edge AI-driven drug discovery environment. The Senior Alliance Manager will oversee alliance governance, align internal and external teams, and ensure successful delivery of collaborative research and development programs. The position plays a key role in scaling operational frameworks and fostering a collaborative culture across high-impact partnerships.

Isomorphic Labs London, United Kingdom

Hybrid Permanent