Senior Clinical Project Manager – Oncology

• Independently lead clinical projects in accordance with the study budget and scope of work.
• Set and achieve objectives for project execution, including contracted and financial objectives.
• Run international trials when required.
• Serve as the primary client point of contact and provide excellent customer service.
• Participate in proposal activities and client presentations.
• Liaise with project teams and senior management at Precision and sponsor organizations, including C-level stakeholders.
• Handle and 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.
• Identify key deliverables, success metrics, and escalation needs.
• Contribute as an active Project Team member to efficient trial management and execution.
• Prepare and review protocols and study documentation, including project plans, informed consents, site contracts, and budgets.
• Manage client relationships, project teams, budgets, timelines, scope, cost, and quality throughout the study lifecycle.

• 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 in 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 with individuals and teams internally and externally.
• Demonstrated core understanding of medical terminology and clinical trial activities as they relate to execution of a clinical development plan.
• Legally authorized to work in the country of employment without employer sponsorship.

• Supportive and collaborative environment
• Work-life balance
• Team development opportunities
• Opportunity to work with a global team
• Equal opportunity employer
• Reasonable accommodation for applicants with disabilities