Senior Clinical Project Manager – Oncology

• Independently lead clinical projects according to study budget and scope of work.
• Set and achieve contracted and financial project objectives.
• Run international trials when required.
• Serve as the primary client liaison and provide excellent customer service.
• Participate in proposal activities and client presentations.
• Liaise with project teams and senior management, including C-level stakeholders, at Precision and sponsor organizations.
• Lead all aspects of clinical research trials.
• Manage all functional areas, including data management, safety, clinical, medical monitoring, and biostatistics.
• Prepare project status updates for clients and management, including deliverables, success metrics, and escalations.
• Contribute to efficient management and execution of trials as an active Project Team member.
• Prepare and review protocols and study documentation, including project plans, informed consents, site contracts, and budgets.
• Oversee clinical project delivery, functional departments, timelines, scope, cost, and quality across global/regional Phase I–IV oncology trials.
• Manage client relationships, project teams, budgets, and timelines throughout the full study cycle, from proposal strategy and costing through completion.

• Degree or similar related life science qualification, or equivalent combination of education and experience.
• Previous experience in a full service/global Project Management role working in the CRO industry is essential.
• Extensive experience working within Clinical Operations within a CRO.
• At least 4 years full service Project Management experience in a clinical trial setting working for 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.
• Effective written and spoken English communication.
• Strong presentation skills.
• Proven computer skills in MS Office, MS Project, and PowerPoint.
• Software experience with CTMS, eTMF, EDC, and IXRS.
• Proven ability to develop positive working relationships internally and externally.
• Core understanding of medical terminology and clinical trial activities related to executing a clinical development plan.
• Must be legally authorized to work in the country of employment without employer sponsorship.

• Supportive and collaborative environment
• Work-life balance
• Team development and growth support
• Opportunity to work with a global team
• Equal opportunity employment
• Reasonable accommodation during the application process