Latest Environmental Risk Assessment Scientist Jobs

GCP Compliance Manager - Clinical Programs & Trials

This role involves providing expert Good Clinical Practice (GCP) compliance guidance to clinical trial teams, supporting decision-making on complex regulatory issues, and ensuring adherence to quality standards across global clinical programs. The manager will lead investigations into quality issues, drive inspection readiness, and translate regulatory requirements into practical actions. Collaboration with cross-functional stakeholders is central to strengthening compliance and fostering a culture of data integrity and accountability.

Novartis London, United Kingdom

Hybrid Permanent

GCP Compliance Manager - Clinical Programs & Trials

This role involves providing expert Good Clinical Practice (GCP) compliance guidance to clinical trial teams, supporting decision-making on complex regulatory issues, leading quality issue resolution, and ensuring inspection readiness across global clinical programs. The manager will translate regulatory requirements into actionable insights, conduct self-assessments, and drive continuous improvement in compliance. Embedded within cross-functional teams, the role emphasizes proactive risk mitigation, data integrity, and collaboration with Quality Assurance and Development functions.

Novartis Ardross, Alba / Scotland, IV17 0YF, United Kingdom

Hybrid Permanent

Process Safety Engineer

This role involves providing expert process safety leadership at GSK’s Barnard Castle manufacturing site, ensuring compliance with EHS regulations and delivering process safety improvements. The engineer will lead hazard assessments, support incident investigations, and drive safe working practices across production operations, with a strong focus on regulatory standards like DSEAR and CDM. The position plays a key part in maintaining safety integrity within a high-value, regulated pharmaceutical environment.

GSK Barnard Castle, United Kingdom

On-site Permanent

Statistics Leader / Associate Director – Oncology Statistics

This role involves leading statistical planning and delivery for clinical programs in oncology, working closely with cross-functional teams to design robust clinical trials and contribute to regulatory strategy. The position also focuses on methodological innovation and mentoring colleagues to build statistical capability and quality.

GSK United Kingdom

Hybrid Permanent

Associate Director Clinical Supply IRT

This role involves leading the onboarding and continuous improvement of IRT standards and studies for AstraZeneca's clinical trials. Responsibilities include technical documentation, risk assessment, test script development, training, and process optimization. The position requires deep knowledge of R&D supply chain, clinical development processes, and IRT systems, with a focus on delivering high-quality, efficient clinical trial supplies.

AstraZeneca Macclesfield, United Kingdom

On-site Permanent

Feasibility and Recruitment Lead

This role involves leading UK feasibility and recruitment for cutting-edge cell therapy studies, translating scientific insights into actionable plans. Responsibilities include guiding end-to-end feasibility, collaborating with global stakeholders, and developing recruitment strategies to ensure timely and effective patient access to trials.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Oncology Medical Head, International

This senior leadership role involves defining and executing the international medical strategy for Pfizer’s Oncology portfolio, collaborating with global teams to ensure patient-centered, evidence-driven medical impact. The role requires deep oncology expertise and strong leadership to drive strategic decisions and medical execution across regions.

Pfizer

On-site Permanent

Oncology Medical Head, International

This role involves defining and executing the international medical strategy for Pfizer’s Oncology portfolio, collaborating with global and regional teams to ensure patient-centered, evidence-driven decisions. The position requires deep oncology expertise and leadership to drive medical impact across international markets.

Pfizer

On-site Permanent

Principal Research Associate, Clinical Biomarker Laboratory, Flow Cytometry

This role involves leading high-parameter spectral flow cytometry activities in a GCLP-compliant clinical laboratory, generating immunophenotyping and functional immune profiling data from PBMC and whole blood samples to support mRNA-based clinical development. The scientist will independently execute and analyze complex assays, contribute to assay development and validation, and ensure regulatory compliance while leveraging advanced platforms like the Cytek Aurora. Opportunities exist to engage with digital tools and generative AI for data interpretation and workflow optimization within a collaborative, innovation-driven environment.

Moderna Oxford, United Kingdom

Hybrid Permanent

Principal Research Associate, Clinical Biomarker Laboratory, Flow Cytometry

This role involves generating and analyzing high-parameter flow cytometry data from clinical trial samples to support immunology research in a GCLP-compliant environment. The scientist will operate advanced spectral flow platforms like the Cytek Aurora, perform ex vivo immune functional assays, and ensure data integrity through rigorous documentation and compliance. Emphasis is placed on innovation through AI-enabled tools, assay development, and mentoring within a collaborative, regulated laboratory setting.

Moderna

Hybrid Permanent

Technical Program Coordinator, DDMR, London

As a Technical Program Coordinator, you will support the Drug Design and Medical Research (DDMR) function by managing program planning, monitoring timelines, tracking actions, and reporting risks. You will work closely with drug design teams, internal stakeholders, and external partners to ensure effective communication and alignment across the organization.

Isomorphic Labs London, United Kingdom

On-site Permanent

Regulatory Affairs Specialist - Medical Devices - Cambridge

This role involves providing regulatory expertise to guide product development across medical and non-medical technologies, ensuring compliance with international standards such as ISO 13485, FDA 21 CFR 820, and ISO 9001. The specialist will work embedded within project teams, interpreting evolving regulations, supporting quality systems, and enabling innovation while maintaining regulatory alignment throughout the product lifecycle.

Newton Colmore Cambridge, Cambridgeshire, United Kingdom

On-site Permanent

Head of Business Development

This role involves leading business development efforts to secure and scale strategic partnerships with pharmaceutical companies. Responsibilities include researching targets, engaging decision-makers, negotiating deals, and creating scalable commercial models for AI-driven biology collaborations. The position requires a strong pharmaceutical network and experience in shaping novel deal structures.

Latent Labs London, United Kingdom, United Kingdom

Hybrid Permanent

Regulatory Affairs Specialist

This role involves maintaining technical documentation and ensuring compliance with UK and EU MDR regulations for Class I and IIa medical devices. The specialist will support regulatory submissions, post-market surveillance, and quality management system development within a regulated environment. Collaboration with the QA Manager and ongoing product lifecycle support are key aspects of the position.

Cure Talent Upper Marlbrook, Worcestershire, B61 0RT, United Kingdom £45,000 – £50,000 pa

On-site Permanent

Regulatory Affairs Manager

Cure Talent are delighted to be partnered with a global medical device organisation recognised as one of the most established and successful healthcare companies in the world. With a diverse international footprint and a strong pipeline of innovation, the business...

Cure Talent Curbridge, Oxfordshire, Oxfordshire, United Kingdom £85,000 – £95,000 pa