CareerPlan

Clinical Trial Manager (Associate Director) - London

London, United KingdomFull-time2026-04-14 → 2026-11-11
On-site

Core

Manage day-to-day operations of clinical trials for biotech and pharmaceutical clients, ensuring compliance with ICH/GCP regulations and serving as the primary operational contact for sponsors.

Role type

Senior IC Clinical Trial Manager (Associate Director)

Builds

Clinical trial projects across phases 1-4 for biotechnology, pharmaceutical, and medical device industries

Domain

Clinical Research / Biopharmaceuticals

Required skills

Clinical Trial Management, Protocol development, Risk assessment, Vendor management, Site quality oversight, Cross-functional team leadership, Regulatory compliance (ICH/GCP)

Preferred skills

Oncology therapeutic area expertise, Phases 2-3 experience, CRO experience, Bid defense experience, Advanced degree in health/life sciences

Technologies

Clinical trial management systems, Regulatory databases

Responsibilities

Manage and provide accountability for day-to-day operations of the project, Serve as primary Sponsor contact for operational project-specific issues, Review and provide input for study protocol and final study report, Develop operational project plans, Manage risk assessment and execution, Manage site quality including supervision of Clinical Research Associates

Seniority

Senior, hands-on IC with management responsibilities