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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 liaison with clients and internal stakeholders including 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, providing excellent customer service and participating in proposals 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 points
- Coordinating cross-functional teams and driving quality across study execution
- Managing domestic and international travel as needed
The company emphasizes a collaborative, people-focused environment that promotes work-life balance and team development, with a particular passion for rare diseases and oncology research.
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 within a CRO environment
- 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 plans
