Our global, full-service CRO seeks an experienced Clinical Project Manager to lead rare disease studies from start to finish. You will oversee complex clinical trials, providing leadership across project teams and ensuring the delivery of high-quality solutions for our biopharma clients.
- Lead and manage rare disease clinical trials from Phase I-IV, including study setup, monitoring, and close-out
- Drive and track study timelines, budgets, recruitment, and milestones
- Lead cross-functional core project teams and ensure alignment on deliverables
- Provide ongoing communication, insight, and guidance to clients
- Identify and mitigate risks, escalating issues appropriately
- Ensure adherence to ICH-GCP, global regulations, SOPs, and processes
- Coach and mentor more junior clinical project management staff
- Bachelor's degree in science or healthcare-related field
- 7+ years overseeing rare disease clinical trials in a full-service CRO
- Expert knowledge of ICH-GCP and global regulatory guidelines
- Excellent leadership, stakeholder management, and communication skills
- Strong problem-solving abilities and attention to detail
- Passion for making a difference in rare disease therapy areas
We offer an excellent compensation and benefits package along with opportunities for career development and growth.
To learn more about this critical rare disease leadership role, contact us today! Candidates must be based in the UK and have full work authorization.