Latest regulatory affairs Jobs

Manager, Labelling Strategy and Development

Lead the development and maintenance of global product labelling, including datasheets, prescribing information, and patient leaflets, ensuring accurate scientific and medical content across international markets. Collaborate with cross-functional teams in regulatory, clinical, safety, and governance to support product lifecycle management and compliance. Mentor team members, maintain documentation in regulatory systems, and contribute to labelling strategy in a complex global environment.

GSK Stevenage, United Kingdom

Hybrid Permanent

Manager, Labelling Strategy and Development

This role involves leading the development and maintenance of global product labelling, including prescribing information and patient leaflets, for pharmaceutical products. The manager will collaborate with cross-functional teams to ensure accurate, compliant, and scientifically sound labelling across international markets, supporting medicines throughout their lifecycle. Key responsibilities include authoring regulatory documents, aligning labelling strategy, and mentoring team members within a global regulatory environment.

GSK United Kingdom

Hybrid Permanent

Senior Manager, HTA, Value and Evidence (HV&E), Rare Disease

This role involves developing and executing high-quality HTA, Value & Evidence strategies to support patient access and reimbursement for Rare Disease treatments. The Senior Manager will manage health economics and outcomes research, collaborate with cross-functional teams, and ensure a consistent evidence generation strategy across markets.

Pfizer United States

On-site Permanent

Senior Manager, HTA, Value and Evidence (HV&E), Rare Disease

This role involves developing and executing high-quality HTA, Value & Evidence strategies to support patient access and reimbursement for Rare Disease treatments. The Senior Manager will lead the generation of health economics and outcomes research, manage global value dossiers, and coordinate with cross-functional teams to ensure a consistent and robust evidence strategy.

Pfizer London, SW7 2AP, United Kingdom

Hybrid Permanent

(Senior) Clinical Development Medical Director

Job Description Summary#LI-HybridWork Arrangement: Hybrid WorkingLocation: London (The Westworks), United KingdomRelocation Support: This role is based in London, United Kingdom. Please only apply if accessible.Are you passionate about shaping the future of clinical development and making a meaningful impact in...

Novartis London, United Kingdom

Clinical Development Medical Director - Neuromuscular

Salary Range:£83,510.00 - £155,090.00Job Description SummaryWork Arrangement: Hybrid, #LI-HybridPrimary Location: London, United KingdomOther Locations: Barcelona, Spain; Dublin, IrelandRelocation Support: This role is based in London, United Kingdom. Novartis is unable to offer relocation support: please only apply if accessible.As Clinical...

Novartis London, United Kingdom

Senior Director Global Clinical Program Lead Cardiovascular & Renal

This role involves leading the clinical development and strategic oversight of a medicine for cardiovascular and renal conditions. Responsibilities include managing the Clinical Development Team, ensuring high clinical and scientific standards, and authoring key study documents and regulatory submissions.

CSL

On-site Permanent

(Fixed Term) Manufacturing Associate I

The Manufacturing Associate will operate production equipment for mRNA vaccines, ensuring compliance with cGMP and safety regulations. Responsibilities include maintaining documentation, troubleshooting equipment, and participating in continuous improvement projects in a fast-paced, team-oriented environment.

Moderna Oxford, United Kingdom

On-site Temporary

Fixed Term Manufacturing Associate II

This role involves operating production equipment for mRNA vaccines, adhering to cGMP and safety regulations, and participating in continuous improvement initiatives. The candidate will work closely with QA teams, troubleshoot equipment issues, and maintain meticulous documentation in a fast-paced, technologically advanced environment.

Moderna Oxford, United Kingdom

On-site Temporary

Sr. Data Platform Engineer - Computer System Validator

In this role, you will build, scale, and operate a validated data platform with petabyte-scale data, ensuring data integrity and traceability in a GxP-compliant environment. You will work closely with biologists, chemists, and data scientists to make diverse datasets discoverable and queryable, supporting Recursion’s drug discovery efforts. Additionally, you will mentor and coach team members, sharing your technical expertise and fostering growth.

Recursion London, United Kingdom £75,900 – £101,900 pa

Hybrid Permanent

Senior Director, Global Product Lead, Early Oncology R&D

This role involves leading global product teams in early oncology R&D, from candidate selection through Phase III investment decisions. Responsibilities include shaping development strategies, engaging stakeholders, and ensuring ethical standards in oncology research.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Senior Director, Search & Evaluation Late TA Lead, Immunology

This role involves leading strategic sourcing and evaluation of late-stage external Hematology therapeutic area opportunities, from Phase 2 through marketed drugs. Responsibilities include engaging with Key Opinion Leaders, driving due diligence, and shaping the portfolio through high-impact partnerships.

CSL United States £263,000 – £328,000 pa

Hybrid Permanent

Sr. Data Platform Engineer - Computer System Validator

As a Senior Data Platform Engineer, you will build, scale, and operate a validated data platform with petabyte-scale data, ensuring data integrity and traceability in a GxP-compliant environment. You will collaborate with biologists, chemists, and data scientists to make Recursion’s vast datasets discoverable and queryable, supporting the company’s mission to advance drug discovery through technology and biology.

Recursion United Kingdom US$142,500 – US$220,500 pa

Hybrid Permanent

Director – Process Design and Optimisation in Chemical Development

This role involves leading a team in the design and optimisation of chemical processes for drug development. Responsibilities include technical direction, project delivery, regulatory submissions, and mentoring scientists. The position leverages innovative technologies and AI to enhance process efficiency and ensure robust commercial processes.

AstraZeneca Macclesfield, United Kingdom

Hybrid Permanent

Global Studies Asset Manager (GSAM)

The Global Asset Study Manager (GASM) at Roche/Genentech is responsible for the efficient execution of global clinical trials, ensuring consistency and compliance with IHC-GCP and Roche processes. Key responsibilities include coordinating study management, developing essential documents, driving innovation, and maintaining inspection readiness.

Roche Welwyn Hatfield, United Kingdom

On-site Permanent