Senior Project Manager - Rare Disease
ProPharma Group · US
Clinical OperationsFull-timeCompany career page
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Role summary
ProPharma Group seeks a Senior Project Manager to oversee rare disease clinical studies from initiation through closeout. The role involves managing timelines, budgets, stakeholder communication, and regulatory compliance while coordinating cross-functional teams and ensuring study execution meets sponsor requirements.
What they're looking for
- Clinical operations project management experience in pharmaceutical or biotech settings
- Knowledge of FDA regulations, ICH-GCP guidelines, and applicable regulatory frameworks
- Demonstrated ability to manage budgets, timelines, and resource allocation
- Strong cross-functional communication and stakeholder management skills
- Experience with clinical trial study plans, TMF management, and study documentation
- Project planning and risk assessment capabilities
What you'll be doing
- Plan and manage clinical studies from initiation to closeout, monitoring timelines and budgets
- Serve as primary communication liaison between clinical, internal, and external project stakeholders
- Develop and maintain study project plans, including site selection, monitoring, and TMF management
- Oversee study drug and supply management, vendor selection, and investigator meeting execution
- Monitor regulatory compliance and develop subject recruitment and retention strategies
Key requirements
- Therapeutic area
- Rare Disease
Privacy & handoff
This role links to ProPharma Group'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.