Clinical Trial Manager (Associate Director) – Stirling

Overview

In this role you drive the day-to-day operations of clinical trials, ensuring compliance and timely delivery within ICH/GCP guidelines. You will serve as the primary Sponsor contact for operational issues and oversee cross-functional teams to meet study milestones. Your deep protocol and therapeutic area knowledge will shape operational plans and risk management. You join a mission-driven CRO that accelerates global development of safe therapeutics and offers flexible work options for relevant experience. You will lead and scale trial operations across Phases 1–4 in a collaborative, impact-focused environment.

Pay / Benefits

• Flexible work environment
• Competitive compensation and benefits package
• Competitive PTO packages
• Structured career paths with opportunities for professional growth
• Company-sponsored employee appreciation events
• Employee health and wellness initiatives

Responsibilities

• Manage day-to-day operations of the project per contract and regulatory requirements
• Serve as primary Sponsor contact for operational issues and study deliverables
• Maintain in-depth knowledge of protocol and therapeutic area
• Provide cross-functional oversight and ensure necessary training for team
• Review and input for study protocol, edit check specs, data analysis plan, and final study report when applicable
• Develop operational project plans
• Manage risk assessment and execution
• Responsible for management of study vendors
• Manage site quality and supervise Clinical Research Associates and monitoring deliverables

Key requirements

• Bachelor’s degree in health or life science field; advanced degree preferred
• 5+ years of Clinical Trial Management experience; CRO experience preferred
• Experience in Phases 1-4 (Phases 2-3 preferred)
• Project/timeline management experience; bid defense experience preferred
• Strong leadership skills

• leadership
• cross-functional collaboration
• communication
• ICH/GCP compliance
• vendor management
• study protocol development

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