Latest Clinical Research Associate Jobs

ViiV Healthcare (GSK) Senior Director, Clinical Development

As a Senior Medical Director at ViiV Healthcare, you will lead the design and delivery of early development plans for HIV treatments, ensuring clinical excellence and medical governance across Phase 1-4 studies. You will collaborate with internal and external stakeholders to design, execute, and interpret clinical studies, focusing on long-acting medicines and ensuring patient safety and data integrity.

GSK United States

On-site Permanent

ViiV Healthcare (GSK) Senior Director, Clinical Development

This role involves leading the design and delivery of early development plans for HIV treatments, ensuring clinical excellence and medical governance across Phase 1-4 studies. You will collaborate with internal and external stakeholders to design, execute, and interpret clinical studies, ensuring patient safety and scientific excellence.

GSK

On-site Permanent

Clinical Development Scientist, Manager

The Clinical Development Scientist (Manager) role involves providing scientific oversight and ensuring data integrity for clinical trials in Internal Medicine. Responsibilities include protocol development, data review, safety monitoring, and contributing to clinical documents and reports. The role also involves supporting site selection, training, and continuous improvement initiatives to enhance clinical trial execution.

Pfizer

On-site Permanent

Clinical Development Scientist, Manager

The Clinical Development Scientist (Manager) role involves providing scientific oversight and ensuring data integrity for clinical trials in Internal Medicine. Responsibilities include protocol development, data review, safety monitoring, and contributing to clinical documents and reports. The role also involves collaborating with various stakeholders, including external committees and site-facing colleagues, to ensure the successful execution of clinical studies.

Pfizer

On-site Permanent

Global Labelling Manager, Content (Neuroscience)

The Global Labelling Manager, Content will lead the development and maintenance of high-quality global labelling documents for pharmaceutical products. Key responsibilities include organising cross-functional discussions, conducting research on competitor labels, and ensuring compliance with regulatory standards across different markets.

Novartis

Hybrid Permanent

GCP Compliance Manager - Clinical Programs & Trials

This role involves providing compliance oversight for clinical programs and trials, ensuring adherence to Good Clinical Practice standards. You will act as a primary compliance partner to Clinical Trial Teams, enabling decision-making on complex regulatory scenarios and leading cross-functional discussions to resolve quality issues.

Novartis Ireland

Hybrid Permanent

Logistics Coordinator – Temperature-Controlled Supply (5 Month Secondment

This role involves supporting the day-to-day logistics activities for clinical studies, ensuring medicines are delivered on time and under the correct temperature conditions. You will manage temperature excursions, coordinate with logistics partners, and contribute to continuous improvement initiatives.

AstraZeneca Macclesfield, United Kingdom

On-site Contract

Associate Principal AI & ML Engineer – Evinova

As an Associate Principal AI & ML Engineer at Evinova, you will develop and integrate advanced algorithms and generative AI systems to optimize clinical trial design and improve drug development processes. Your role involves working with multi-source data, building production systems, and collaborating with cross-functional teams to drive impactful solutions.

AstraZeneca London, United Kingdom

Hybrid Permanent

Director, Search & Evaluation Early TA Lead (CVR and Haem)

This role involves leading strategic sourcing and evaluation of external innovation opportunities in Hematology and Cardiovascular/Renal therapeutic areas. Responsibilities include identifying high-potential assets, shaping early partnering strategies, and driving transactions in collaboration with Business Development. The role requires deep scientific expertise and a strong network within biotech, academia, and pharma BD organizations.

CSL

On-site Permanent

Director, Search & Evaluation Early TA Lead (CVR and Haem)

This role involves leading the strategic sourcing and evaluation of external innovation opportunities in Hematology and Cardiovascular/Renal therapeutic areas. Responsibilities include identifying high-potential assets, shaping early partnering strategies, and driving transactions in collaboration with Business Development.

CSL

On-site Permanent

Quality Engineer (Compliance)

This role involves ensuring medical device and drug-device combination products meet strict regulatory standards throughout development. The Quality Engineer (Compliance) will lead design controls, risk management, and audit readiness activities, working closely with development teams and external partners. Key focus areas include DHF and RMF maintenance, regulatory compliance, and supporting clinical trial investigations.

Next Phase Recruitment Cambridge, Cambridgeshire, United Kingdom

Hybrid Contract

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

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

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