Latest clinical research associate Jobs

Senior Principal Biostatistician

This role involves leading the implementation of innovative trial designs and statistical models, collaborating with clinical and regulatory teams, and contributing to exploratory analyses and statistical consultations. The position requires a strong background in biostatistics and the ability to drive quantitative decision-making in clinical trials.

Novartis London, United Kingdom

Hybrid Permanent

Trial Vendor Associate Director

This role involves managing all clinical vendor-related aspects of global clinical trials, including vendor service delivery, contract negotiations, cost control, and user-acceptance testing for eCOA and IRT systems. You will collaborate closely with the study team and ensure vendor service excellence throughout the trial lifecycle.

Novartis United Kingdom

Remote Permanent

Metabolite Identification Specialist

This role involves leading metabolite identification and biotransformation studies to determine the metabolic fate of drug candidates. The specialist will design and interpret advanced analytical data using techniques like high-resolution mass spectrometry, support drug discovery and development programmes, and provide scientific guidance to project teams and junior scientists. The position emphasizes technical leadership, problem-solving in complex metabolic pathways, and direct contribution to the progression of pharmaceutical candidates.

SRG Sandwich, United Kingdom

On-site Permanent

Specialist Biomedical Scientist

Who we're looking for:* You must be a HCPC registered Biomedical Scientist with no restrictions on practice* You must be experienced in either Blood Transfusion, Haematology or Chemical Pathology* 2 years' experience post state registration experience is essential* Excellent communication...

Spire Healthcare Southampton, Hampshire, SO19 8NJ, United Kingdom

Regulatory Affairs Assistant

The Regulatory Affairs Assistant will provide administrative, operational, and compliance support to the Regulatory Affairs team, ensuring accurate data and documentation, supporting team processes, and maintaining compliance with regulatory standards. The role involves a broad range of activities, including regulatory file compilation, database management, project coordination, and administrative support to the Head of Regulatory and the team.

AstraZeneca London, United Kingdom

On-site Permanent

Senior Computational Biologist, Tooling

In this role, you will work on the Value Tech Tooling Team at the forefront of drug discovery, using massive data capabilities to develop and maintain robust data pipelines and analytical workflows. You will collaborate with a cross-functional team of computational biologists, engineers, and scientists to turn complex analyses into reusable tools and pipelines, accelerating the discovery of life-changing therapeutics.

Recursion London, United Kingdom

On-site Permanent

Associate Director, Regulatory Project Manager

Lead global regulatory project planning and execution across CSL’s product portfolio, ensuring timely submissions and alignment with strategic initiatives. Oversee cross-functional teams, drive process improvements, and ensure compliance with global health authority requirements. Mentor junior staff and contribute to governance and standardization in regulatory operations.

CSL US$170,000 – US$210,000 pa

Hybrid Permanent

Associate Director, Regulatory Project Manager

Leads global regulatory project planning and execution across CSL’s product portfolio, overseeing submission coordination and cross-functional collaboration to meet health authority requirements. Drives process improvements and operational excellence within regulatory operations, aligning initiatives with strategic priorities. Mentors junior staff and supports standardization of regulatory processes across regions.

CSL US$170,000 – US$210,000 pa

Hybrid Permanent

Associate Director, Regulatory Project Manager

This role leads global regulatory project planning and execution across CSL’s biologics product portfolio, overseeing end-to-end regulatory submissions and cross-functional collaboration. The individual will manage project timelines, risk, and compliance while driving process improvements and mentoring junior staff. Work involves close coordination with regulatory, clinical, manufacturing, and policy teams to meet global health authority requirements.

CSL US$170,000 – US$210,000 pa

Hybrid Permanent

Principal Scientist, TechBio Discovery

Your work will change lives. Including your own.The Impact You'll MakeRecursion is at the forefront of reimagining drug discovery by integrating technological innovations across biology, chemistry, automation, data science, and engineering to radically improve lives by industrializing drug discovery. We...

Recursion North Tyneside, NE29 8EP, United Kingdom US$198,000 – US$271,700 pa

Hybrid Permanent

Head of Medicinal Chemistry, Drug Design, London

As Head of Medicinal Chemistry, you will lead a team of 25 chemists in London, driving the development of novel drugs using cutting-edge AI and machine learning. You will provide strategic direction, mentor team members, and collaborate with AI/ML scientists to accelerate drug discovery and clinical candidate nomination.

Isomorphic Labs London, United Kingdom

On-site Permanent

Principal Scientist, TechBio Discovery

Your work will change lives. Including your own.The Impact You'll MakeRecursion is at the forefront of reimagining drug discovery by integrating technological innovations across biology, chemistry, automation, data science, and engineering to radically improve lives by industrializing drug discovery. We...

Recursion United Kingdom £198,000 – £271,700 pa

Hybrid Permanent

Regulatory Conformance Officer (12-month / Secondment)

As a Regulatory Conformance Officer, you will ensure that GSK's products meet all licensing and regulatory requirements, maintaining compliance with global market authorisations and supporting regulatory submissions. You will collaborate with multiple functions, including manufacturing, R&D, and global regulatory affairs, to deliver regulatory strategies and inspection readiness.

GSK Barnard Castle, United Kingdom

On-site Contract

Medical Affairs Partner - Nephrology & Rheumatology

Acts as a key medical affairs liaison for nephrology and rheumatology, translating complex scientific data into strategic initiatives and fostering relationships with healthcare experts. Supports local and global medical strategies, contributes to scientific partnerships, medical education, and insight generation. Works within a collaborative, patient-focused environment to improve healthcare outcomes.

Roche Welwyn Hatfield, United Kingdom

Hybrid Contract

Senior Scientist – 12-month - Pharmaceutical Sciences

This role involves developing analytical control strategies and methodologies to support the manufacturing of clinical active pharmaceutical ingredients (APIs) for both small molecules and novel modalities like oligonucleotides and peptides. The scientist will work within the Early Chemical Development (ECD) group, collaborating with chemists and external partners to interpret complex data, improve processes, and ensure compliance with GMP and safety standards. The position emphasizes innovation, scientific rigor, and the application of advanced technologies including AI and automation.

AstraZeneca Macclesfield, United Kingdom

On-site Contract