Latest Therapeutics Jobs

Associate Director - Global Regulatory Affairs (Oncology Therapeutic Group)

Develops and executes global and regional regulatory strategies for oncology assets, ensuring optimal labelling, approvals and lifecycle compliance. Partners with the Global Regulatory Lead, therapeutic area head and cross-functional teams to shape development plans and regulatory authority interactions across multiple regions, while driving process improvement and innovation.

GSK Baar Onyx €98,250 – €163,750 pa

Hybrid

Associate Director - Global Regulatory Affairs (Oncology Therapeutic Group)

Develops and executes global and regional regulatory strategies for oncology assets, ensuring optimal labelling, approvals and lifecycle compliance. Partners with the Global Regulatory Lead and cross-functional teams on submissions, health-authority interactions and regulatory intelligence across multiple regions. Hybrid role based in London, Stevenage, Baar or Wavre.

GSK Wavre, Belgium €98,250 – €163,750 pa

Hybrid

Clinical Program Director Early Development Oncology

Leads global operational delivery of early development oncology programs, managing Clinical Project Managers, Monitoring Leads and CTAs. Owns the clinical development plan, CRO and site selection strategy, budgets and timelines, and serves on Asset Teams. Requires deep first-in-human and Phase I oncology trial expertise.

Ipsen London

Hybrid

Director, Regulatory Affairs, Labelling

Lead global labelling strategy for assigned products across early and late-stage development, lifecycle management and marketed portfolios, serving as Therapeutic Area Lead. Drive core labelling documents including CCDS, USPI and EU PI, lead health authority negotiations, and shape a future USPI operating model while championing digitalisation and AI-enabled labelling solutions.

Ipsen London

Global Safety Lead - Formulation Safety

Provides medical and scientific expertise on clinical safety across the full product lifecycle, with emphasis on evaluating safety data during clinical development and post-approval. Chairs the Safety Management Team, oversees signal detection, aggregate reports (DSURs, PSURs, RMPs) and regulatory responses, and sets safety strategy for global cross-functional development and post-marketing teams.

CSL Maidenhead

Global Safety Lead - Formulation Safety

Provides medical and scientific expertise on clinical safety across a product's lifecycle, with emphasis on signal detection, risk management and regulatory submissions. Chairs the Safety Management Team, oversees aggregate reports such as DSURs, PSURs and RMPs, and acts as the safety representative in cross-functional development and post-marketing teams.

CSL Opfikon, Switzerland

Research Leader (DMPK), Cambridge, MA

Lead DMPK strategy across drug discovery projects, designing screening cascades and mechanistic experiments while integrating DMPK, PD and toxicology data for dose and safety predictions. Work closely with AI/ML platform teams to optimise computational ADME models and author regulatory sections, in a hybrid Cambridge, MA role.

Isomorphic Labs Cambridge, United States

Hybrid

Research Leader (Toxicology), Cambridge, MA

Lead the safety assessment strategy for small molecule and biologic drug discovery projects from inception to regulatory submission, designing screening cascades and mechanistic experiments. Partner with machine learning researchers to build predictive toxicology models and manage CRO relationships for outsourced wet-lab data generation, while mentoring junior team members.

Isomorphic Labs Cambridge, United States

Hybrid

Associate Director / Director, Biostatistics

Provides strategic statistical leadership for Health Technology Assessment, pricing, reimbursement and market access across assigned programmes, partnering with value & access, HEOR, medical affairs and RWE teams. Leads HTA methods such as population adjustment, evidence synthesis, survival extrapolation and causal inference, supports payer and JCA dossiers, and mentors biostatisticians while overseeing outsourced work.

Novartis London £83,510 – £155,090 pa

Hybrid

Don't see what you're looking for?

A general expression-of-interest posting inviting candidates to join a talent network rather than apply for a specific role. Applicants submit a resume to be kept on file and contacted when a suitable opening arises across the company's AI-driven drug discovery operations. No defined day-to-day responsibilities, team or technology stack are described.

Recursion Salt Lake City, United States

Global Site and Study Operations Contracting Undergraduate

A 12-month industrial placement within Pfizer's Global Site and Study Operations, focused on drafting and negotiating clinical trial site contracts and budgets. The undergraduate works with an experienced Site Contracting Team Lead, gaining exposure to legal terms, regulatory requirements and process improvement projects across therapeutic areas.

Pfizer United Kingdom - Sandwich

On-site Internship

Manager, Medical Writing, Immunology

Leads the preparation and finalisation of clinical documents within the Regulatory Medical Writing team, supporting the Immunology therapeutic area. Takes a lead role on assigned projects for content, scientific strategy, timing and tracking, and manages direct reports including hiring, goal-setting and development. Involves guiding cross-functional teams, peer review and maintaining knowledge of ICH and regulatory guidelines.

Johnson & Johnson Innovative Medicine Maidenhead

Associate Director, CMC Regulatory Science, International

Leads CMC regulatory strategy for global submissions including IND, CTA, BLA and MAA, and oversees agency correspondence and compliance for mRNA products. Reviews submissions for readiness, drives health authority interactions, and advises manufacturing and quality teams on change controls and regulatory guidance across vaccines, oncology and rare disease programmes.

Moderna London

On-site Permanent Clearance Required

Regulatory Affairs Manager

Deliver and maintain UK competitive licences, lead regulatory strategy for new initiatives, and ensure compliance across defined products and projects. Provide local regulatory expertise for clinical trial approvals, lifecycle submissions and MHRA interactions, contributing to cross-functional teams and study feasibility work.

AstraZeneca London

Permanent

Senior Manager, Real-World Data Research

An individual contributor role conducting non-interventional real-world data research for medical and HEOR teams across international markets. You will identify data sources, oversee statistical programming in R, and interpret and present findings to stakeholders. The position requires deep expertise in observational data analysis and offers hybrid working from Uxbridge.

Bristol Myers Squibb Uxbridge

Hybrid