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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 in accordance with study budgets and scope, serve as the primary client liaison, and manage relationships with internal teams and C-level stakeholders at both Precision and sponsor organizations.
Key responsibilities include:
- Leading clinical projects from proposal strategy through completion, including costing, bid defense, and full-cycle execution
- Serving as primary point-of-contact for clients, providing excellent customer service and participating in proposal activities and presentations
- Managing all aspects of clinical research trials, including protocol reviews, study documentation (informed consents, site contracts, budgets), and project plans
- Preparing project status updates identifying key deliverables, performance metrics, and escalation points
- Coordinating cross-functional teams with both internal and external stakeholders to drive quality and efficient execution
- Managing budgets, timelines, and international trial operations, with availability for domestic and international travel
The company emphasizes a collaborative, high-energy environment focused on rare diseases and oncology, with a commitment to work-life balance and team development.
Requirements:
- Degree or equivalent qualification in life sciences or related field, or equivalent combination of education and experience
- Minimum 4 years of full-service project management experience in clinical trial settings within a CRO
- Extensive experience in clinical operations roles within a CRO
- Demonstrated experience managing oncology studies
- Working understanding of GCP/ICH guidelines and the clinical development process
- Strong English language communication skills (written and spoken) and presentation abilities
- Proven computer proficiency: MS Office, MS Project, PowerPoint, and clinical software (CTMS, eTMF, EDC, IXRS)
- Ability to develop positive working relationships internally and externally
- Demonstrated understanding of medical terminology and clinical trial activities
- Availability for domestic and international travel including overnight stays
