Clinical Project Manager

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.