Clinical Trial Manager II
ICON · Warsaw, Poland +5 more
Clinical OperationsFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
ICON seeks a Clinical Trial Manager II to oversee sponsor-dedicated study operations across multiple European locations. The role involves designing trials, managing enrollment, ensuring regulatory compliance, and coordinating cross-functional teams. Requires a life sciences degree, 5+ years of study management experience, and expertise in GCP/ICH guidelines and clinical development processes.
What they're looking for
- Bachelor's degree in life sciences or related discipline
- 5+ years of study management experience in pharmaceutical/scientific environment
- In-depth knowledge of GCP and ICH guidelines
- Experience in clinical research including study management, monitoring, data management
- Project management skills with ability to manage scope, budget, timeline, resources
- Leadership skills with ability to motivate and empower team members
- Willingness to travel approximately 25% as required
What you'll be doing
- Oversee clinical trial management workstreams and ensure deliverables meet quality and timeline expectations
- Collaborate with cross-functional teams to design, implement, and manage clinical trial protocols and enrollment
- Analyze and interpret clinical trial data to identify trends and optimize study outcomes
- Ensure compliance with ICH/GCP guidelines, regulatory standards, and company SOPs for assigned studies
- Manage study budgets, vendor oversight, stakeholder communication, and multiple trial deliverables including TMF filing and patient engagement
Privacy & handoff
This role links to ICON's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.