Latest Life Sciences Jobs

Director, AI/ML MIDD Oncology Clinical Pharmacology, Modeling and Simulation

Lead clinical pharmacology and modelling & simulation efforts for oncology drug development, applying AI/ML and quantitative methods to optimise dosing, trial design, and regulatory strategy. Drive innovation in model-informed drug development across small molecules, biologics, and antibody-drug conjugates. Collaborate with cross-functional teams to accelerate therapies to patients using advanced pharmacometric and machine learning techniques.

GSK £188,100 – £313,500 pa

Safety Scientist – SERM (Safety Evaluation and Risk Management)

A Safety Scientist in GSK's Safety Evaluation and Risk Management (SERM) team is responsible for evaluating safety signals, contributing to risk management plans, and ensuring patient safety across clinical development and post-marketing phases. The role involves analyzing safety data from multiple sources, authoring regulatory reports, and collaborating with cross-functional teams to identify and mitigate risks. It requires strong scientific and medical expertise in pharmacovigilance within a global regulatory environment.

GSK PLN 215,250 – PLN 358,750 pa

Bioanalytical Lead, London

Lead the development and execution of bioanalytical strategies for a diverse portfolio of AI-designed therapeutics, including small molecules, biologics, and ADCs. Design and validate PK, PD, and immunogenicity assays, manage global CROs, and integrate bioanalytical data into AI models to refine drug discovery. Play a key role in IND-enabling studies and cross-functional preclinical development in a hybrid London-based role.

Isomorphic Labs London, United Kingdom

Hybrid Permanent

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

Clinical Development Medical Director - Neuromuscular

Leads global clinical development programs in neuroscience, with a focus on neuromuscular or related disorders. Provides medical and scientific leadership across trial design, regulatory submissions, data interpretation, and external engagement. Works cross-functionally to drive innovative therapies from concept to approval, with emphasis on gene therapy and complex clinical data.

Novartis Ireland €90,300 – €167,700 pa

Hybrid Permanent

Associate Director, Regulatory Diagnostics

This role involves designing and delivering global regulatory strategies for precision diagnostics, including companion diagnostics and in vitro devices, within drug development programs. The individual will lead regulatory submissions across the lifecycle, engage with health authorities, and ensure compliance with global regulations. Collaboration with cross-functional teams and external partners is central to advancing regulatory plans for innovative diagnostics in a hybrid working environment.

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

Hybrid Permanent

R&D Consultant - Drug Delivery Device Design - Cambridge

Lead the design and development of innovative drug delivery devices through early-stage concept creation, prototyping, and experimental design. Work within multidisciplinary teams to translate technical challenges into manufacturable medical solutions while advising clients on development pathways and regulatory considerations. Play a hands-on role in R&D leadership and technical mentorship.

Newton Colmore Cambridge, Cambridgeshire, United Kingdom

On-site Permanent

Global Development Lead, Internal Medicine, Sr. Director (MD)

Leads clinical development for assigned assets in Internal Medicine, serving as the primary clinical accountability point within Pfizer's Research & Development. Designs and oversees global clinical trials, regulatory submissions, and cross-functional team coordination, with potential involvement in obesity-related late-stage programs. Engages with external stakeholders and ensures compliance with scientific, regulatory, and safety standards.

Pfizer England

On-site Permanent

Global Development Lead, Internal Medicine, Sr. Director (non-MD)

This role involves leading clinical development for Internal Medicine assets within Pfizer's Research & Development division, with a focus on obesity-related therapies. The Global Development Lead will design and oversee global clinical trials, create development plans, and ensure regulatory compliance across regions including China and Japan. The position requires cross-functional leadership, engagement with external stakeholders, and contribution to regulatory submissions and product labeling.

Pfizer England £214,900 – £358,100 pa

On-site Permanent