Latest Pharmaceutical Scientist Jobs

Medical Director-Oncology Clinical Development - GI

This role involves leading medical monitoring and safety oversight for gastrointestinal (GI) oncology clinical trials, ensuring patient safety and clinical integrity. The Medical Director provides physician-level input into study design, data interpretation, and regulatory interactions, working closely with cross-functional teams and external experts. It emphasizes integration of medical expertise across clinical development, with a focus on advancing cancer treatments through innovative science and collaboration.

GSK £222,750 – £371,250 pa

Medical Director-Oncology Clinical Development - GI

This role involves leading medical monitoring and safety oversight for gastrointestinal (GI) oncology clinical trials within GSK’s global development programme. The Medical Director provides physician-level expertise in study design, data interpretation, and regulatory engagement, ensuring patient safety and clinical integrity across phases I–III. Working within a cross-functional matrix team, the role integrates medical insight into clinical strategy and collaborates with external experts and investigators to advance innovative cancer therapies.

GSK

Hybrid Permanent

Director of Nonclinical Safety, Cambridge, MA

Lead the development and execution of nonclinical safety strategies for small molecule drug candidates in oncology and non-oncology programs, integrating AI-driven predictive models with traditional toxicology. Build and scale the nonclinical safety function within an AI-first drug discovery environment, ensuring high-quality data feedback to refine computational models. Collaborate across preclinical, clinical, and regulatory teams to advance compounds through IND and NDA/MAA-enabling studies.

Isomorphic Labs Cambridge, United Kingdom

Field Service Engineer, Medical Diagnostic Systems

Provide on-site service, maintenance, and breakdown repair for advanced medical diagnostic systems used in NHS and private laboratories. Work directly with laboratory staff to resolve technical issues and ensure optimal system performance. Receive full product training and support a market-leading provider of diagnostic equipment.

TRS Consulting Falkirk, Stirling And Falkirk, United Kingdom £52,000 pa

Field Service Engineer, Medical Diagnostic Systems

Perform on-site service and repair of advanced medical diagnostic systems in NHS and private laboratories, ensuring minimal downtime through proactive maintenance and technical troubleshooting. Work closely with lab personnel to deliver reliable diagnostic solutions while receiving full product training. Role involves frequent customer visits and some weekend work as part of a five-day working week.

TRS Consulting Stirling, Stirling And Falkirk, United Kingdom £52,000 pa

Quality Manager (m/f/x) - EU-based

The Quality Manager role involves maintaining and improving CSL's quality management systems across Europe and global affiliates. Responsibilities include inspection readiness, process harmonization, and supporting quality initiatives. The role requires collaboration with multiple functions and stakeholders, with a focus on compliance and continuous improvement.

CSL

Quality Manager (m/f/x) - EU-based

The Quality Manager role involves maintaining and improving CSL's quality management systems across Europe and global affiliates. Responsibilities include coordinating inspection readiness, supporting compliance activities, and implementing global quality initiatives. The role requires strong knowledge of pharmaceutical regulations and quality systems, with a focus on collaboration and process improvement.

CSL

Director, International HEOR & HTA, Immunology

This role involves developing and executing HEOR and HTA strategies for Novartis' Immunology portfolio, ensuring payer and HTA evidence requirements are integrated into clinical development plans. You will partner with various teams to maximize asset value and translate complex evidence into compelling value stories for healthcare decision-makers.

Novartis London, United Kingdom

Global Regulatory Associate Director, Life Cycle Management

This role involves managing regulatory maintenance activities for a high-complexity pharmaceutical product portfolio, ensuring compliance and timely submissions to global health authorities. The individual will lead strategic regulatory input across cross-functional teams, respond to complex queries, and support continuous process improvements. It is a hybrid or remote position with a focus on lifecycle management of innovative medicines.

Novartis £67,900 – £126,100 pa

Hybrid Permanent

Vice President, Medical Affairs

The Vice President, Medical Affairs, will lead the development and execution of integrated medical strategies for Recursion's clinical portfolio, focusing on areas like oncology, rare disease, and immunology. Key responsibilities include building evidence-generation plans, engaging with key opinion leaders, and ensuring compliance with medical and regulatory standards.

Recursion United Kingdom

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Senior Engineer, CSV Validation

This role involves end-to-end ownership of computerised system validation (CSV) for GxP-regulated systems used in the manufacturing and testing of advanced CAR-T cell therapies. The engineer will author and execute validation documentation, ensure compliance with international regulations (e.g. FDA 21 CFR Part 11, EU GMP Annex 11), manage change controls and CAPAs, and support regulatory inspections. The position requires strong technical writing, cross-functional collaboration, and expertise in GAMP 5 and data integrity within a biopharmaceutical context.

Autolus Stevenage, United Kingdom

Executive Director, Asset Team Lead

The Executive Director, Asset Team Lead, will drive the strategic positioning of clinical assets in oncology and immunology, leveraging Recursion's proprietary OS and ClinTech insights. This role involves cross-functional collaboration to ensure the advancement of transformative medicines, with a focus on competitive positioning and patient benefit.

Recursion United Kingdom

Regulatory Specialist

The Regulatory Specialist will ensure product compliance across various regulatory frameworks, prepare and maintain technical documentation, and liaise with regulatory authorities. The role offers flexible working hours and remote options, making it suitable for candidates with experience in highly regulated industries like chemicals, pharmaceuticals, and medical devices.

Extension Recruitment North Seaton, Northumberland, NE63 9YW, United Kingdom £50,000 – £52,000 pa

Hybrid Permanent Part-time

Clinical Development Leader

This role involves leading global clinical strategy for Roche’s toxicology and drug testing portfolio, including designing and executing high-impact clinical development programs. The Clinical Development Leader will drive regulatory interactions, integrate real-world evidence, and collaborate with key opinion leaders to advance diagnostic innovations. The position emphasizes scientific leadership, cross-functional collaboration, and mentoring within a globally distributed team.

Roche United States US$138,700 – US$257,500 pa

Clinical Development Leader

Leads global clinical strategy for Roche’s toxicology and drug testing portfolio, designing and executing clinical development programs to support regulatory approval and market adoption. Acts as scientific authority in interactions with health agencies, drives real-world evidence integration, and collaborates with KOLs and cross-functional teams to advance diagnostic innovation. Focuses on generating robust clinical evidence to demonstrate safety, effectiveness, and scientific validity of diagnostic solutions.

Roche US$138,700 – US$257,500 pa