Latest regulatory affairs Jobs

Senior Medical Director, Oncology Clinical Development - GU

This role involves leading clinical development for oncology assets, specifically in genitourinary (GU) cancers, within a global matrix environment. The Senior Medical Director will design and execute phase 1–3 clinical trials, provide medical oversight, interpret study data, and engage with external experts and regulatory authorities. The position plays a key strategic role in advancing GSK’s oncology pipeline from development through regulatory approval and lifecycle management.

GSK US$284,250 – US$473,750 pa

On-site Permanent

Head, Oncology Clinical Development - ADCs

Leads end-to-end clinical development of an antibody-drug conjugate (ADC) oncology asset across multiple tumor types, from first-in-human through registrational trials and launch. Responsible for shaping clinical strategy, overseeing global trials, engaging with regulatory authorities, and integrating translational research and innovative approaches like AI/ML and real-world evidence. Acts as senior clinical representative in governance forums and external scientific engagements.

GSK Stevenage, United Kingdom US$242,250 – US$403,750 pa

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

Associate Director, CMC Regulatory Science, International

Lead the development and execution of CMC regulatory strategies for mRNA-based products across global submissions, including IND/CTA/BLA/MAA filings. Provide expert guidance on regulatory compliance, interact with health authorities, and support quality and manufacturing teams through change controls and submissions. Work within a multidisciplinary team at the Harwell site to advance Moderna’s pipeline in vaccines, oncology, and rare diseases.

Moderna London, United Kingdom

On-site Permanent

Associate Director, Global Regulatory Science, CMC

This role leads global regulatory CMC strategy for mRNA-based medicines, developing and implementing regulatory plans for international submissions. The individual will guide CMC documentation, interact with health authorities, and provide strategic input across product development stages, ensuring compliance with EU and global regulations. The position plays a key part in advancing Moderna’s pipeline of transformative therapeutics across vaccines, oncology, and rare diseases.

Moderna

Hybrid Permanent

GCP Compliance Director (Program & Study)

Lead a team of GCP Compliance Managers to ensure global clinical trials adhere to Good Clinical Practice and regulatory standards. Drive inspection readiness, audit oversight, and quality issue management across clinical development programs. Shape compliance strategy and foster a culture of quality and continuous improvement within a matrixed pharmaceutical environment.

Novartis London, United Kingdom £83,510 – £155,090 pa

Hybrid Permanent

Senior Director, Search & Evaluation Late TA Lead, Immunology

This role involves leading strategic sourcing and evaluation of late-stage external Hematology therapeutic assets, engaging with key opinion leaders, and integrating innovation into portfolio planning. The position requires deep clinical expertise, a proven track record in deal-making, and strong collaboration with cross-functional teams.

CSL US$263,000 – US$328,000 pa

Hybrid Permanent

Senior Director, Search & Evaluation Late TA Lead, Immunology

Lead the strategic sourcing and evaluation of late-stage therapeutic assets in Immunology, Hematology, or related areas, from Phase 2 through marketed drugs. Drive cross-functional due diligence, engage with key opinion leaders and clinical networks, and shape portfolio strategy through high-impact partnerships and transactions. Operate within a global biotech ecosystem with strong collaboration across R&D, BD, and regulatory functions.

CSL US$263,000 – US$328,000 pa

Hybrid Permanent

Research Leader (Toxicology), Cambridge, MA

This role involves leading toxicology strategy in drug discovery with an AI-first approach, designing safety assessment frameworks, and guiding the development of predictive AI models for toxicity. The candidate will work across small molecules and biologics, collaborate with machine learning teams, oversee outsourced wet-lab studies via CROs, and mentor junior scientists. A key focus is reducing reliance on animal testing through innovative, data-driven toxicology solutions.

Isomorphic Labs Cambridge, United Kingdom

Associate Director, Translational Medicine, Oncology, Cambridge, MA

Lead the development and execution of translational medicine strategies for oncology programs, integrating AI-driven insights to inform clinical trial design and biomarker development. Collaborate with cross-functional teams to translate preclinical findings into clinical applications and advance companion diagnostics. Play a key role in shaping the scientific direction of early-stage drug development using cutting-edge methodologies and digital biology approaches.

Isomorphic Labs Cambridge, United Kingdom

Field Service Engineer - Medical Diagnostics - South Region - Exeter - London - Kent

Perform on-site and remote technical support for Roche’s diagnostic systems, including troubleshooting, preventive maintenance, and customer training across the South Region. Use advanced diagnostic tools to resolve electro-mechanical faults and ensure regulatory compliance. Work within a customer-centric team to maximise system uptime and operational efficiency in clinical environments.

Roche United Kingdom

Field Service Engineer - Medical Diagnostics -Central Region Wales, Wirral and East Anglia

This role involves providing on-site and remote technical support for Roche’s diagnostic systems across medical laboratories and healthcare facilities. You’ll troubleshoot electro-mechanical faults, perform preventive maintenance, and deliver training to ensure optimal system uptime and customer proficiency. The position emphasizes compliance, reporting, and collaboration within a customer-centric field support team.

Roche United Kingdom

Asset Manager

The Asset Manager will lead the strategic and operational management of EIT's physical asset portfolio, including laboratories, scientific facilities, and office spaces. Key responsibilities include developing an asset management strategy, maintaining an accurate asset register, overseeing the asset lifecycle, and implementing predictive maintenance practices to support future growth and compliance.

Ellison Institute of Technology Oxford, United Kingdom

On-site Permanent

Scientist, Small Molecular Chemist - Plant Biology Institute

This role involves conducting high-impact research in plant specialised metabolism engineering, focusing on the development of novel decarbonised plant-based production of food and medicines. The scientist will work in a collaborative environment, designing and conducting experiments, developing customized libraries, and driving the translation of research into real-world solutions.

Ellison Institute of Technology Oxford, United Kingdom

On-site Permanent

TCTU Portfolio Trial Manager (BE-GENOMICS)

This role involves managing clinical trials, including providing support on approval processes, trial management, recruitment strategies, and data quality. The position is part of the Tayside Clinical Trials Unit (TCTU) and focuses on both new and established drug and complex intervention trials, with a lead role in the BE-Genomics trial.

University of Dundee Dundee, United Kingdom £37 – £46 pa

On-site Contract Part-time