Latest Clinical Research Associate Jobs

Pfizer logo

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 providing clinical support to study teams and investigators.

Pfizer
Pfizer logo

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 providing clinical support to study teams and investigators.

Pfizer
GSK logo

Medical Director, Oncology Clinical Development

The Medical Director, Oncology Clinical Development will lead clinical research activities for GSK’s oncology portfolio, collaborating with various stakeholders to develop and execute phase 1-3 clinical trials. Key responsibilities include protocol development, medical monitoring, safety data review, and strategic partnerships with key external experts.

GSK Stevenage, United Kingdom
Hybrid Permanent
GSK logo

Medical Director, Oncology Clinical Development

The Medical Director, Oncology Clinical Development will lead clinical research activities, develop and execute oncology clinical trials, and engage with key external experts. Responsibilities include protocol development, medical monitoring, safety data review, and collaborating with various stakeholders to advance GSK’s clinical portfolio.

GSK
Hybrid Permanent
AstraZeneca logo

Director, Alliance Management

This role involves leading strategic partnerships with CROs, ensuring governance, performance, and relationship management. The Director will collaborate globally, drive continuous improvement, and support cross-functional teams at AstraZeneca's Cambridge Biomedical Campus.

AstraZeneca Cambridge, United Kingdom
Hybrid Permanent
AstraZeneca logo

Medical Director, Senior Patient Safety Physician

This role involves leading the clinical safety strategy for drug projects and products, ensuring the safety and risk management of AstraZeneca's pharmaceuticals. You will work on evaluating adverse events, communicating safety data, and contributing to regulatory submissions, all while collaborating with a global team of experts.

AstraZeneca Chatham, ME4 4NP, United Kingdom
Hybrid Permanent Flexible
Recursion logo

Research Synthesis Chemist

Your work will change lives. Including your own.The Impact You’ll MakeWe are growing our chemistry team at Recursion and are seeking a Research Synthetic Chemist to join our Automated Chemistry group. We are looking for an individual that thrives in...

Recursion Crathes, Alba / Scotland, United Kingdom

Scientific Programme Administrator, Clinical Genomics

The role involves supporting the delivery of high-quality genomics-based External Quality Assessment (EQA) schemes, working closely with scientific and operational teams to ensure accurate and reliable genetic test results. Responsibilities include sample preparation, data handling, quality management, and laboratory support, contributing to international standards in diagnostic genomics.

MFK Recruitment Salford, Manchester, M41 8PH, United Kingdom £32,442 pa
Hybrid Permanent

Mechanical Design Engineer

Cure Talent are delighted to be partnered with an emerging wearable medical technology company at an exciting stage of its growth. Developing next generation wearable medical devices designed to deliver clinically meaningful physiological insights beyond the hospital environment, the business...

Cure Talent Loughborough, Leicestershire, LE11 2QG, United Kingdom £30,000 – £40,000 pa
NHS Professionals logo

Band 6 Specialist Biomedical Scientist Chemical Pathology

Job summary We have an exciting opportunity for a Specialist Biomedical Scientist in Clinical Biochemistry/Immunology. The service supports all hospital wards and departments, as well as GPs, clinics, and private hospitals across central and south Buckinghamshire and beyond. The central...

NHS Professionals Walton, Buckinghamshire, Buckinghamshire

Senior Software Engineer

This role involves developing the software ecosystem for a next-generation wearable medical device, focusing on SDKs, desktop applications, and third-party integrations. You will work closely with firmware, hardware, and data science teams to ensure robust, compliant software solutions for clinical studies and commercial deployment.

Cure Talent Hathern, Leicestershire, LE12 5LA, United Kingdom £60,000 – £80,000 pa
On-site Permanent

Field Service Engineer, Medical Diagnostic Systems

This role involves servicing and repairing sophisticated medical and laboratory diagnostic systems used in pathology departments and NHS laboratories. You will visit customer sites, troubleshoot issues, and liaise with laboratory managers and technicians. Full product training is provided.

TRS Consulting Crawley, West Sussex, United Kingdom £45,000 – £48,000 pa
On-site Permanent

Field Service Engineer, Medical Diagnostic Systems

Field Service Engineer, Medical Diagnostic SystemsBasic Salary Up To £50,000Overall Earnings £60,000+Bonus 15%£10 Per Day Lunch AllowanceCompany CarPensionHealthcareLife InsurancePhone, LaptopHolidaysThe Role – Field Service Engineer, Medical Diagnostic SystemsThis market leader seeks to recruit a technically motivated and customer focused Field...

TRS Consulting Holbeck, West Yorkshire, LS11 9LY, United Kingdom £50,000 pa
On-site Permanent
Isomorphic Labs logo

Head of Computational Drug Design, Cambridge, MA

Isomorphic Labs is applying frontier AI to help unlock deeper scientific insights, faster breakthroughs, and life-changing medicines with an ambition to solve all disease.The future is coming. A future enabled and enriched by the incredible power of machine learning. A...

Isomorphic Labs Cambridge, United Kingdom
Isomorphic Labs logo

Senior Technical Program Manager (Preclinical), London

This role involves managing the non-clinical aspects of IND submissions, including CMC, DMPK, pharmacology, and tox reporting. You will create and maintain detailed project plans, manage data and document workflows, and coordinate cross-functional teams to ensure regulatory compliance and successful submission.

Isomorphic Labs London, United Kingdom
On-site Permanent