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
• Run international trials as needed
• Serve as primary client point of contact and provide customer service
• Participate in proposal activities and client presentations
• Liaise with project teams and senior management, including 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, identify deliverables and performance metrics, and escalate issues
• Contribute to efficient management and execution of trials
• Prepare and review protocols and study documentation, including project plans, informed consents, site contracts, and budgets
• Provide full-service oversight for global and regional Phase I-IV oncology trials
• 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
• 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
• Proven 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 executing 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
• Professional growth support
• Equal Opportunity Employer
• Reasonable accommodation for applicants with disabilities