Senior Clinical Project Manager – Oncology

• Independently lead clinical projects according to study budget and scope of work
• Set and achieve contractual and financial project objectives
• Manage international trials when required
• Serve as primary client point of contact and provide customer service
• Participate in proposal activities and client presentations
• Liaise with project teams, senior management, sponsors, and C-level stakeholders
• Lead all aspects of clinical research trials
• Manage functional areas including data management, safety, clinical, medical monitoring, and biostatistics
• Prepare project status updates, key deliverables, performance metrics, and escalations
• Contribute to efficient management and execution of trials
• Prepare and review protocols and study documentation, including project plans, informed consents, site contracts, and budgets
• Coordinate cross-functional internal and external stakeholders and drive study quality
• Oversee clinical project delivery, timelines, scope, cost, and quality across global or regional Phase I–IV oncology trials
• Participate in proposal strategy, development, costing, bid defense, and full-cycle study completion
• Manage client relationships, project teams, budgets, and timelines

• 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
• Extensive experience in Clinical Operations within a CRO
• At least 4 years of 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
• Computer skills in MS Office, MS Project, and PowerPoint
• Software experience with CTMS, eTMF, EDC, and IXRS
• Ability to develop positive working relationships internally and externally
• Core understanding of medical terminology and clinical trial activities related to execution of 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 opportunities
• Equal Opportunity Employer
• Reasonable accommodation available for applicants with disabilities