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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 of work, 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 development, costing, and bid defense
- Managing client relationships, project teams, and budgets throughout the study lifecycle
- Preparing and reviewing protocols, project plans, informed consents, site contracts, and budgets
- Generating project status updates for clients and management, identifying key deliverables and performance metrics
- Coordinating cross-functional teams and driving quality across study execution
- Handling all aspects of clinical research trials, including international trials requiring travel
- Serving as an active member of the project team to ensure efficient trial management and execution
Precision for Medicine is described as a people-focused CRO with a supportive, collaborative environment that promotes work-life balance and team development. The company combines novel clinical trial designs, operational and medical expertise, advanced biomarker and data analytics, and a focus on rare diseases and oncology.
**Requirements:**
- Degree or equivalent qualification in life sciences (or equivalent combination of education and experience)
- Previous experience in a full-service/global project management role within a CRO is essential
- Minimum 4 years of full-service project management experience in a clinical trial setting at a Clinical Research Organisation
- 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: CTMS, eTMF, EDC, IXRS
- Demonstrated ability to develop positive working relationships with individuals and teams internally and externally
- Core understanding of medical terminology and clinical trial activities as they relate to clinical development plan execution
- Legal authorization to work in the country of employment without employer sponsorship
