Clinical Project Manager / Senior Clinical Project Manager - Clinical Trial Services

About the Role A role to provide full-service leadership of oncology-focused clinical projects across global/regional Ph I-IV trials, with end-to-end oversight of study delivery, cross-functional teams, and client relationships. What You'll Do

• Independently lead clinical projects in accordance with study budget and scope of work.
• Use strong interpersonal and organizational skills to set and achieve objectives, including contracted and financial objectives.
• May be called upon to run international trials.
• Serve as primary client liaison, including participation in proposal activities and client presentations.
• Liaise with Project Team and senior management of Precision and sponsors, including C-level.
• Handle and lead all aspects of a clinical research trial or trials.
• Provide total project management for all functional areas: data management, safety, clinical, medical monitoring, biostatistics, etc.
• Prepare project status updates for clients and management; identify key deliverables and performance metrics; escalate as needed.
• Be an active member of the Project Team to contribute to efficient trial management and execution.
• Prepare and review protocols and study documents such as project plans, informed consents, site contracts and budgets. What We're Looking For
• Degree or life sciences qualification, or equivalent combination of education and experience.
• Experience in a full-service/global PM role in the CRO industry.
• Extensive experience in Clinical Operations within a CRO; at least 4 years of full-service PM experience in clinical trials.
• Experience managing oncology studies.
• Working understanding of GCP/ICH guidelines and the clinical development process.
• Ability to travel domestically and internationally with overnight stays.
• Effective English communication (written and spoken); strong presentation skills.
• Proficient in MS Office, MS Project, PowerPoint, and systems such as CTMS, eTMF, EDC, IXRS.
• Demonstrated ability to build positive internal and external relationships; solid understanding of medical terminology and clinical trial activities related to a development plan. Compensation & Benefits
• We promote a people-focused CRO culture with a supportive, collaborative environment that values work-life balance and team development. We offer opportunities to learn, grow, and contribute to cutting-edge oncology trials.