Clinical Pharmacology Trial Leader (trial Leadership) – Translational Medicine
Stellen Nordrhein Westfalen
London, UK
Hybrid
Clinical pharmacology trial leadership
First-in-human and early phase studies
Collaboration with contract research organisations
This position plays a critical role in the delivery of first-in-human and clinical pharmacology studies, representing a major step in the development of new medicines
Job Summary
This position plays a critical role in the delivery of first-in-human and clinical pharmacology studies, representing a major step in the development of new medicines.
You will act as the primary bridge between Novartis and the selected Contract Research Organisations conducting the clinical pharmacology study, providing clear direction, oversight and integration from protocol development through to Clinical Study Report delivery.
This is a highly collaborative, hands-on role, requiring strong study leadership, excellent communication skills and confidence operating at the interface between internal teams and external partners.
Matching Summary
This position plays a critical role in the delivery of first-in-human and clinical pharmacology studies, representing a major step in the development of new medicines.
Skills & Requirements
Must-have
Clinical pharmacology trial leadership
First-in-human and early phase studies
Collaboration with Contract Research Organisations
Protocol development and study design
Clinical data interpretation including PK/PD
Cross-functional team coordination
High quality clinical trial conduct
Nice-to-have
Strong communication skills
Hands-on study leadership
Ability to manage complexity and ambiguity
Growth mindset and team contribution
Fostering collaboration and accountability
Key Requirements
Bachelor’s degree in life sciences or healthcare
Advanced degree preferred (MSc, PhD, PharmD, MD or equivalent)
Approximately 2+ years experience for Clinical Pharmacology Trial Leader
Approximately 6+ years experience for Senior Clinical Pharmacology Trial Leader
Experience leading first-in-human and clinical pharmacology studies
Strong knowledge of ICH GCP and regulatory requirements
Work permit not supported for this role
Work Rights
Work permit not supported; must have right to work in UK