Position Summary
We are seeking an experienced Clinical Project Manager (CPM) to lead and oversee global clinical trials. The ideal candidate will bring both strategic oversight and hands-on leadership to ensure studies are delivered on time, within scope, and in compliance with all regulatory and ethical standards.
Key Responsibilities
- Lead and plan, execution, and delivery of Phase I–IV clinical trials in Parkinson’s disease.
- Serve as the primary sponsor contact for assigned studies, ensuring strong communication and partnership.
- Develop and manage project timelines, budgets, risk assessments, and mitigation strategies.
- Oversee CRO/vendor selection, contract negotiations, and ongoing performance management.
- Ensure protocol adherence, GCP compliance, and data integrity across all study sites.
- Collaborate cross-functionally with Clinical Operations, Data Management, Biostatistics, and Regulatory Affairs teams.
- Support site selection, feasibility assessments, and investigator relationships within the Parkinson’s research network.
- Mentor and guide project team members to foster professional growth and ensure cohesive execution.
Qualifications
- Bachelor’s degree in Life Sciences, Nursing, or related field (advanced degree preferred).
- 5+ years of clinical project management experience in a CRO, biotech, or pharma environment.
- Proven track record of successful delivery of global or multi-center clinical trials.
- Strong knowledge of ICH-GCP, FDA, and EMA regulations.
- Excellent organizational, leadership, and communication skills.
