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Precision for Medicine, a CRO specializing in precision medicine and oncology, is seeking an experienced Senior Clinical Project Manager to lead full-service clinical trial projects across global and regional Phase I-IV oncology studies.
In this role, you will have end-to-end oversight of clinical project delivery, managing all functional departments (data management, safety, clinical, medical monitoring, biostatistics) and ensuring adherence to agreed timelines, scope, cost, and quality standards. You will independently lead projects from proposal strategy and costing through bid defense and study completion, serving as the primary client liaison and managing relationships with internal teams, external stakeholders, and C-level executives.
Key responsibilities include:
- Leading clinical projects in accordance with study budgets and scope of work
- Serving as primary point-of-contact for clients, including proposal activities and presentations
- Managing all aspects of clinical research trials, including protocol reviews, informed consents, site contracts, and budget preparation
- Preparing project status updates identifying key deliverables, performance metrics, and escalation issues
- Coordinating cross-functional teams to drive quality and efficient trial execution
- Managing international trials and availability for domestic and international travel
You will work in a collaborative, high-energy environment with a team dedicated to advancing cancer therapies and rare disease research.
Requirements:
- Degree or equivalent qualification in life sciences or related field
- Minimum 4 years of full-service project management experience in clinical trial settings within a CRO
- Extensive experience in clinical operations within a CRO environment
- Demonstrated experience managing oncology studies
- Working understanding of GCP/ICH guidelines and clinical development processes
- Strong presentation and communication skills (written and spoken English)
- Proficiency in MS Office, MS Project, PowerPoint, and clinical trial software (CTMS, eTMF, EDC, IXRS)
- Proven ability to develop positive working relationships internally and externally
- Core understanding of medical terminology and clinical trial activities
- Availability for domestic and international travel including overnight stays
