Jobs in London

Global Labelling Director (Team Lead), Content

Leads a team of labelling professionals to develop and maintain global labelling strategies and content for pharmaceutical products. Ensures compliance with regulatory requirements and alignment with product development and lifecycle plans through close collaboration with cross-functional teams and regulatory authorities. Focuses on continuous improvement of labelling processes and high-quality, science-driven documentation.

Novartis London, United Kingdom
Hybrid Permanent

Global Labelling Associate Director, Content (Established Products)

Leads the development and maintenance of global labelling strategies and core documents for pharmaceutical products, ensuring scientific accuracy and regulatory compliance. Facilitates cross-functional alignment, supports health authority interactions, and mentors team members. Focuses on consistent, competitive product information across global markets.

Novartis
Hybrid Permanent
Recursion logo

Associate Director, Computational Biology – Early Discovery

Lead a team of computational biologists to identify and validate novel oncology targets using integrated phenomics, transcriptomics, genomics, and proteomics data. Develop and scale methods for target discovery in oncology and immunological diseases, collaborating closely with biologists, data scientists, and engineers. Drive data strategy and present findings to stakeholders to advance drug discovery programs.

Recursion United Kingdom
On-site Permanent
Isomorphic Labs logo

Associate Director, Clinical Program Management, Cambridge, MA

The Clinical Program Manager will lead the transition of internal drug programs from pre-IND stages into clinical trial execution, coordinating cross-functional global teams and managing timelines, budgets, and vendor partnerships. The role leverages AI and emerging technologies to drive efficient clinical development with a focus on high-probability outcomes. It involves strategic oversight of CROs and collaborators while ensuring alignment between clinical objectives and company goals.

Isomorphic Labs England
Hybrid Permanent
Isomorphic Labs logo

Medical Director, Clinical Development (Oncology), Cambridge, MA

Leads clinical development strategy for oncology programs, translating AI-driven insights into actionable trial designs and serving as medical monitor. Collaborates with cross-functional teams to advance drug candidates from discovery through proof-of-concept, with responsibility for regulatory submissions and engagement with health authorities and key opinion leaders.

Isomorphic Labs England
Hybrid Permanent
Recursion logo

Director, Clinical Pharmacology

Lead clinical pharmacology and pharmacometrics strategy across rare disease and oncology programs, designing studies and supporting regulatory submissions. Oversee modeling and simulation to inform dose selection and development decisions, working closely with cross-functional teams in a TechBio environment powered by AI-driven drug discovery. Serve as the primary expert in regulatory interactions related to clinical pharmacology.

Recursion London, United Kingdom £118,300 – £136,500 pa
Hybrid Permanent

Global Labelling Associate Director, Content (Oncology)

This role involves leading the development and maintenance of global labelling strategies and core documents for oncology products, ensuring scientific accuracy and regulatory compliance. The individual will facilitate cross-functional alignment, analyse regulatory and competitor data, and support health authority interactions. Based remotely or in London, the position plays a key part in shaping product information across global markets.

Novartis
Hybrid Permanent

Global Labelling Manager, Content (Neuroscience)

This role involves leading the development and maintenance of global core labelling documents for neuroscience products, ensuring accuracy, compliance, and consistency across markets. The individual will facilitate cross-functional alignment, conduct competitor and regulatory research, and support implementation of labelling updates throughout the product lifecycle. Collaboration with regulatory, clinical, and safety teams is central to maintaining high-quality, audit-ready documentation.

Novartis
Hybrid Permanent

Senior Clinical Development Medical Director

This role involves providing clinical leadership and strategic medical input for cardiovascular/stroke drug development programs, including designing and executing global clinical trials. The Senior Clinical Development Medical Director will act as the global medical lead, interpreting clinical and safety data, contributing to regulatory submissions, and collaborating with cross-functional teams and external stakeholders. The position plays a key role in shaping clinical strategy and ensuring patient safety across the development lifecycle.

Novartis

Global Labelling Associate Director, Content (Cardiovascular, Renal & Metabolism)

This role involves leading the development and maintenance of global labelling strategies and core documents for pharmaceutical products in the cardiovascular, renal, and metabolism therapeutic areas. The individual will work cross-functionally to align labelling content, interpret clinical data, and ensure compliance with global regulatory standards. Key responsibilities include supporting health authority interactions, mentoring team members, and maintaining scientific accuracy across product lifecycles.

Novartis London, United Kingdom
Hybrid Permanent

Global Labelling Associate Director, Content (Cardiovascular, Renal & Metabolism)

This role involves developing and maintaining global labelling strategies and core documentation for pharmaceutical products in the cardiovascular, renal, and metabolism therapeutic areas. The individual will lead cross-functional discussions, ensure regulatory compliance, and translate clinical data into accurate, consistent labelling content for global markets. They will also support health authority interactions and contribute to risk assessment and audit readiness.

Novartis
Hybrid Permanent

Clinical Development Medical Director - Neuromuscular

Leads global clinical development programs in neuroscience, with a focus on neuromuscular or related disorders. Provides medical leadership across trial design, regulatory submissions, and safety monitoring, collaborating with cross-functional teams and external stakeholders. Plays a strategic role in advancing innovative therapies through clinical execution and scientific insight.

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

GCP Excellence Monitoring Lead

This role leads the implementation of data-driven, adaptive monitoring strategies across global clinical trials to enhance trial quality and efficiency. The position shapes monitoring standards, tools, and governance frameworks while driving innovation through analytics and technology. It involves leading change initiatives and collaborating with cross-functional teams to improve clinical trial oversight at scale.

Novartis London, United Kingdom £67,900 – £126,100 pa

Translational Medicine Expert – Dermatology, Associate Director

This role involves providing medical and scientific leadership in translational medicine for dermatology programs, spanning early to late-stage drug development. The expert will design and implement strategies for clinical pharmacology, biomarker development, and regulatory submissions, while leading cross-functional teams and supporting in-licensing opportunities. Work includes oversight of clinical studies, publication strategy, and engagement with regulatory and external stakeholders.

Novartis London, United Kingdom £67,900 – £126,100 pa
Hybrid Permanent

Trial Master File Oversight Manager

This role involves overseeing the quality and completeness of global Trial Master Files (TMF) for clinical trials, ensuring compliance and audit readiness. The manager will lead vendor oversight, identify documentation risks, drive remediation, and support continuous improvement in TMF processes. Collaboration with cross-functional teams and stakeholders is central to maintaining high standards in clinical documentation.

Novartis London, United Kingdom £49,140 – £91,260 pa
Hybrid Permanent