Senior Clinical Lead
ProPharma Group · Raleigh
Clinical OperationsFull-timeCompany career page
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Role summary
ProPharma Group seeks a Senior Clinical Lead to oversee site management and clinical monitoring activities across the complete study lifecycle. The role involves leading clinical teams, ensuring regulatory compliance, maintaining stakeholder relationships, and managing quality deliverables for biotech and pharmaceutical clients.
What they're looking for
- 5+ years clinical research experience, including CRA work
- Prior LCRA and/or Clinical Lead experience preferred
- Bachelor's degree or equivalent education and experience
- Advanced CRA capabilities and demonstrated team leadership
- Proficiency with Microsoft Office and clinical trial systems (eTMF, CTMS, EDC, DCT)
- Strong understanding of GCP, ICH Guidelines, SOPs, and regional regulations
- Excellent verbal, written, and interpersonal communication skills
What you'll be doing
- Oversee investigator site management and clinical monitoring teams during study startup, execution, and closeout phases
- Serve as lead site management resource for clients, investigational sites, and internal study teams
- Develop and deliver study-specific training materials for clinical monitoring teams
- Review and approve site visit reports; conduct quality co-monitoring visits to ensure data quality and performance metrics
- Collaborate with clinical project management on study plans, templates, and site initiation; supervise direct report personnel as appropriate
Privacy & handoff
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