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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 all aspects of clinical research trials from proposal strategy through completion
- Participating in proposal activities, client presentations, and bid defense
- Managing project budgets, timelines, and contracted objectives
- Preparing and reviewing protocols, project plans, informed consents, site contracts, and budgets
- Generating project status updates identifying key deliverables, performance metrics, and escalation points
- Coordinating cross-functional teams and driving quality across study execution
- Managing international trials and supporting domestic and international travel as needed
The company emphasizes a collaborative, high-energy environment with a focus on work-life balance and team development. You will work with a dedicated team passionate about advancing cancer therapies and rare disease research.
REQUIREMENTS:
- Degree or equivalent life science qualification (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 clinical development processes
- 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 trial software (CTMS, eTMF, EDC, IXRS)
- Proven ability to build positive working relationships internally and externally
- Core understanding of medical terminology and clinical trial activities related to clinical development planning
