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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 projects, accountable for delivery, functional department coordination, and ensuring adherence to timelines, scope, cost, and quality targets. You will be involved in all study stages—from proposal strategy and development through costing, bid defense, and completion—managing client relationships, project teams, and budgets throughout the trial lifecycle.
Key responsibilities include:
- Independently leading clinical projects in accordance with study budgets and scope of work
- Serving as the primary client liaison, providing excellent customer service and participating in proposals and presentations
- Liaising with project teams and senior management (including C-level) at both Precision and sponsor organizations
- Managing all aspects of clinical research trials, including oversight of data management, safety, clinical monitoring, and biostatistics
- Preparing project status updates identifying key deliverables, performance metrics, and escalation points
- Reviewing protocols and study documentation including project plans, informed consents, site contracts, and budgets
- Contributing as an active project team member to ensure efficient trial execution
- Managing international trials and domestic/international travel as needed
You will work in a cross-functional environment with both internal and external stakeholders, driving quality and coordinating study teams in a collaborative, high-energy setting.
Requirements:
- Degree or equivalent qualification in life sciences or related field, or equivalent combination of education and experience
- Essential: Previous experience in a full-service/global project management role within a CRO
- At least 4 years of full-service project management experience in a clinical trial setting at a Clinical Research Organisation
- Demonstrated experience managing studies within oncology
- Working understanding of GCP/ICH guidelines and the clinical development process
- Ability to drive and availability for domestic and international travel including overnight stays
- Fluent English communication (written and spoken)
- Strong presentation skills
- Proven computer skills: MS Office, MS Project, PowerPoint
- Software experience with 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 planning
- Legal authorization to work in the country of employment without employer sponsorship
