Clinical Trials Supply Manager

About the role

Our client, a global pharmaceutical company, is seeking a Clinical Trials Supply Manager to join their UK team on a 12‑month contract, with the possibility of extending to two years. This remote‑first position offers the chance to work within a centre of excellence that drives innovation in clinical research, while requiring occasional travel to London (approximately two days per month).

Key responsibilities

• Manage clinical supply strategies for trials, ensuring timely and cost‑efficient delivery.
• Create clinical development timelines and proactively resolve potential issues.
• Support drafting of medical protocols and development of package and label outlines.
• Serve as the primary point of contact for clinical supplies, liaising with external vendors and service providers.
• Guarantee that all products comply with protocol specifications and global regulatory requirements.

Required profile

• Strong knowledge of clinical supply chains and drug development processes within the pharmaceutical industry.
• Understanding of global regulatory requirements.
• Experience planning and managing clinical study strategies.
• Good familiarity with IVRS and CTMS systems.
• Excellent communication and analytical abilities.

Required skills

• IVRS
• CTMS

What we offer

• Annual equivalent salary of £50‑52K (paid on an hourly rate).
• Remote‑first work arrangement with limited travel to London.
• 12‑month fixed‑term contract, extendable up to two years.