Associate Director, Clinical Trial Lead (all genders)

Overview

In this role you will own the end-to-end clinical operations strategy and delivery for Phase I–IV studies, including registrational trials. You will lead large global trial teams within a matrix setup, ensuring on-time, budget-conscious, high-quality execution. You will maintain regulatory compliance (ICH-GCP) and drive risk management, governance, and continuous improvement. The position requires on-site presence in Feltham, UK three days per week, and offers engagement with cross-functional partners to advance patient outcomes and organizational goals. You will mentor colleagues, contribute to strategic initiatives, and partner with senior stakeholders to spark discovery and elevate human进

Responsibilities

• own end-to-end clinical operations strategy and delivery for Phase I–IV and registrational trials
• lead large global trial teams in a matrix environment, aligning stakeholders across functions
• manage clinical operational budgets, timelines, and quality standards per governance
• align trial activities with organizational and program strategy goals
• assess and mitigate operational risks using diverse internal and external data
• serve as a clinical operations mentor and best-practice resource
• ensure study management complies with SOPs, instructions, and regulatory guidance (ICH-GCP)
• lead audit activities and participate in non-study-related initiatives and updates to senior management
• contribute to strategic projects with a high degree of creativity and innovation
• on-site collaboration and leadership across global programs to support patient outcomes

Key requirements

• 8+ years in clinical research in CRO or pharmaceutical/biotechnology settings
• 7+ years in clinical trial management with managerial responsibility
• expert experience across multiple therapeutic areas
• strong project management experience with market and competitor awareness
• expert in study planning, startup, budgeting, and resource planning
• ability to lead end-to-end trial activities from start-up to final study report
• strong leadership and influencing capabilities
• effective oral and written communication
• ability to foster cross-project partnerships
• advanced degree desirable (MPH, MS, MA, MBA, PharmD); PM certification desirable

• leadership and people management
• influencing and stakeholder management
• collaboration and cross-functional teamwork
• clinical trial management across Phase I–IV
• budget and resource planning for trials
• start-up activities and study planning

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