Latest Clinical Research Associate Jobs

Clinical Development Medical Director- Hepatology

Lead clinical development for hepatology assets within GSK’s Respiratory, Immunology & Inflammation Research Unit, driving translational research and early-phase clinical trials to validate novel liver disease targets. Provide medical oversight, design clinical development plans, and collaborate cross-functionally to advance innovative therapies from discovery through development. Work in a hybrid model with significant scientific leadership and regulatory engagement responsibilities.

GSK

Clinical Development Medical Director - Cardiovascular

For candidates seeking to be located at our Stevenage site, this role will temporarily be based at Stevenage. However, the Company plans to relocate its offices to Cambridge. The location of this role will therefore subsequently change to Cambridge in...

GSK Stevenage, United Kingdom

Senior Clinical Development Medical Director

Salary Range:£96,036.50 - £178,353.50Job Description Summary#LI-HybridWork Arrangement: Hybrid WorkingLocation: London (The Westworks), United KingdomAre you passionate about shaping the future of clinical development and making a meaningful impact in Cardiovascular/Stroke medicine? We are looking for an experienced and visionary Senior...

Novartis London, United Kingdom

(Senior) Clinical Development Medical Director

A Senior Clinical Development Medical Director will lead cardiovascular clinical programs, providing strategic medical input and ensuring regulatory and safety compliance. The role involves guiding clinical trial execution, collaborating with global teams, and translating scientific data into development pathways. Expertise in cardiovascular drug development and global regulatory processes is essential.

Novartis London, United Kingdom

Hybrid Permanent

Global Development Lead, Internal Medicine, Sr. Director (non-MD)

Leads clinical development for Internal Medicine assets within Pfizer's R&D organization, with end-to-end accountability for creating and executing global clinical development plans. Serves as the primary clinical point of contact across cross-functional teams and external partners, driving trial design, regulatory submissions, and lifecycle strategy. Focuses on obesity and related therapeutic areas, integrating innovation, patient engagement, and regulatory expertise to advance drug development.

Pfizer £214,900 – £358,100 pa

On-site Permanent

Global Development Lead, Internal Medicine, Sr. Director (non-MD)

Leads clinical development for assigned internal medicine assets within Pfizer's Research & Development division, with end-to-end accountability for creating and executing global clinical development plans. Oversees cross-functional teams to design and deliver clinical trials supporting regulatory submissions, while providing therapeutic expertise in obesity and endocrinology. Engages external stakeholders and contributes to regulatory strategy, safety reporting, and product labeling.

Pfizer £214,900 – £358,100 pa

On-site Permanent

Sr. Manager, Site Budgets and Contracts

The RoleReporting to the Director, Global Clinical Operations (GCO) Business Analytics & Operations Management (BAOM), the Senior (Sr.) Manager, Site Budgets & Contracts will focus on the generation and review of investigator site budgets related to investigator grants (IGs) using...

Moderna Oxford, United Kingdom

Sr. Manager, Site Budgets and Contracts

The RoleReporting to the Director, Global Clinical Operations (GCO) Business Analytics & Operations Management (BAOM), the Senior (Sr.) Manager, Site Budgets & Contracts will focus on the generation and review of investigator site budgets related to investigator grants (IGs) using...

Moderna

Lecturer in Biomedical Science (Education and Scholarship)

Deliver and develop undergraduate and postgraduate biomedical science programmes with a focus on innovative teaching and curriculum design. Contribute to pedagogic research, outreach, and professional development within a collaborative academic environment. Integrate expertise as an HCPC-registered scientist into student learning experiences.

Keele University Keele, Midlands Of England, United Kingdom £48 – £58 pa

Permanent

Regulatory Affairs Intelligence Director

This role focuses on transforming regulatory intelligence into strategic decisions that accelerate drug development and approvals. The individual will analyze global regulatory trends, guidance, and precedents to inform pipeline strategy and influence policy, working closely with cross-functional teams and senior leaders. Key responsibilities include conducting in-depth research, providing impact assessments, and integrating emerging technologies like AI into regulatory intelligence processes.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Field Service Engineer, Medical Diagnostic Systems

Perform on-site service and breakdown repair of advanced medical diagnostic systems in NHS and private laboratory settings. Provide technical troubleshooting support and collaborate with lab managers and technicians. Receive full product training and work a five-day week including some weekends.

TRS Consulting Aldershot, Hampshire, GU11 1BX, United Kingdom £52,000 pa

Field Service Engineer, Medical Diagnostic Systems

Perform installation, maintenance, and repair of advanced medical diagnostic systems in NHS and private laboratories. Provide on-site technical support and troubleshooting, working closely with lab staff across diverse healthcare settings. Role includes extensive field work with full product training provided.

TRS Consulting Winchester, Hampshire, United Kingdom £52,000 pa

On-site Permanent

Director, Regulatory Affairs

Lead global regulatory strategy and execution for drug development programs, ensuring compliance across jurisdictions including the US, EU, and UK. Collaborate with cross-functional teams to prepare and manage regulatory submissions such as INDs, NDAs, and orphan drug designations. Provide strategic guidance on regulatory risks and lifecycle management, while engaging with health authorities and shaping regulatory science in the context of AI-driven drug discovery.

Recursion North Tyneside, NE29 8EP, United Kingdom £207,500 – £280,720 pa

Remote Permanent

Data Curator, London

The role involves curating and integrating large-scale biomedical and biochemical datasets to create high-quality, machine learning-ready data assets for AI-driven drug discovery. The Data Curator will work closely with AI and drug discovery teams to improve data quality, interoperability, and representation of chemical, biological, and clinical information. A key focus is leveraging domain expertise in life sciences to enhance training data for predictive and generative AI models.

Isomorphic Labs London, United Kingdom

On-site Permanent

Senior Scientist – Peptide discovery, Biologics Engineering

This role involves leading end-to-end peptide discovery campaigns using in vitro display technologies such as mRNA, phage, yeast, and ribosome display. The scientist will design and optimize diverse peptide libraries, apply NGS and AI-driven analysis for sequence prioritization, and develop automated workflows to accelerate discovery. Working in a multidisciplinary team, they will translate data into high-quality therapeutic candidates while advancing platform capabilities for biologics engineering.

AstraZeneca Cambridge, United Kingdom