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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 globally. You will have end-to-end oversight of Phase I–IV oncology trials, managing all functional departments (data management, safety, clinical, medical monitoring, biostatistics) and ensuring delivery against agreed timelines, scope, cost, and quality metrics.
Key responsibilities include:
- Independently lead clinical projects in accordance with study budgets and scope of work, managing both contracted and financial objectives
- Serve as primary liaison with clients, providing excellent customer service and participating in proposal activities and presentations
- Manage all aspects of clinical research trials from proposal strategy through completion, including costing, bid defense, and full-cycle delivery
- Oversee project teams and budgets, coordinate cross-functional stakeholders (internal and external), and drive quality across study execution
- Prepare project status updates identifying key deliverables, performance metrics, and escalation paths
- Review and prepare protocols, project plans, informed consents, site contracts, and budgets
- Liaise with senior management and C-level executives at both Precision and sponsor organizations
- Support international trial execution and manage domestic/international travel as needed
The role offers a collaborative, high-energy environment focused on rare diseases and oncology research, with emphasis on 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 a clinical trial setting within a CRO
- Extensive experience in clinical operations roles within a CRO setting
- Demonstrated experience managing studies within oncology
- Working understanding of GCP/ICH guidelines and the clinical development process
- Ability to travel domestically and internationally, including overnight stays
- Fluent English (written and spoken)
- Strong presentation skills
- Proficiency with MS Office, MS Project, PowerPoint, and clinical software (CTMS, eTMF, EDC, IXRS)
- Proven ability to develop positive working relationships internally and externally
- Core understanding of medical terminology and clinical trial activities as they relate to clinical development plans
