About this role
About the Role The Clinical Project Manager / Senior Clinical Project Manager will provide full-service oversight for oncology clinical trials (Phases I-IV) across global/regional scopes within a CRO environment. You will lead study delivery, manage cross-functional teams, and oversee timelines, scope, budget and quality, from proposal and costing to bid defense and study completion. What You'll Do
- Independently lead clinical projects in accordance with study budget and scope of work, including potentially international trials.
- Act as primary client liaison, providing excellent customer service and participating in proposals and client presentations.
- Liaise with project team and senior management of Precision and sponsors (including C-level).
- Manage all aspects of a clinical trial or trials across data management, safety, clinical, medical monitoring, biostatistics, etc.
- Provide total project management for all functional areas; monitor milestones, deliverables, and costs.
- Prepare project status updates for clients and management; identify key deliverables and success metrics and escalations.
- Be an active member of the project team to drive efficient management and execution.
- Prepare and review protocols and other study documents such as project plans, informed consent forms, site contracts and budgets.
- Involved in study stages including proposal strategy, development, costing, and bid defense; lead the end-to-end cycle. What We're Looking For
- Degree in life sciences or equivalent; or combination of education and experience.
- Significant experience in a full-service/global PM role within CRO.
- Extensive experience in Clinical Operations within a CRO; at least 4 years PM in clinical trials.
- Oncology trial management experience.
- Strong knowledge of GCP/ICH and the clinical development process.
- Ability to travel domestically and internationally (overnight stays).
- Proficient in English (written and spoken).
- Strong presentation skills.
- Proficient with MS Office, MS Project, PowerPoint; experience with CTMS, eTMF, EDC, IXRS.
- Proven ability to build positive relationships with individuals and teams.
- Solid understanding of medical terminology and clinical trial activities as they relate to the development plan. Compensation & Benefits
- The posting highlights a high-energy, dedicated, collaborative team environment, opportunities for involvement across proposal activities and client interactions, and a focus on work-life balance and team development. No specific salary range is disclosed in the posting.