Clinical Project Manager / Senior Clinical Project Manager

Overview

In this role you will lead full-service oncology clinical projects within a CRO setting, overseeing global and regional trials from proposal strategy to study completion. You will manage client relationships, budgets, timelines, and cross-functional teams to ensure quality and timely delivery. The position emphasizes leadership, coordination across departments, and driving value for sponsors in a dynamic, collaborative environment. This is a chance to influence trial execution at scale in oncology and contribute to precision medicine.

Pay / Benefits

• work life balance
• supportive environment
• team development

Responsibilities

• Provide end-to-end project leadership for global and regional phase I–IV oncology trials within a CRO framework
• Own client relationship management and participate in proposal activities, budgeting, and bid defense
• Coordinate and oversee all functional areas (data management, safety, clinical, medical monitoring, biostatistics)
• Prepare and present project status updates, deliverables, and performance metrics
• Develop and review protocols, project plans, informed consent documents, site contracts, and budgets
• Serve as a liaison between sponsors, Precision for Medicine leadership, and project teams
• Lead cross-functional study teams and ensure adherence to timelines, scope, and quality
• Drive execution and operational efficiency across the full clinical development lifecycle
• Contribute to study design and strategy discussions and support international trial activities

Key requirements

• Degree or similar life science qualification, or equivalent experience
• Extensive full-service/global PM experience in CROs
• 4+ years of clinical project management in a CRO setting
• Experience managing oncology studies
• Strong knowledge of GCP/ICH and clinical development processes
• Ability to travel domestically and internationally
• Excellent English communication and presentation skills
• Proven computer skills (MS Office, MS Project, PowerPoint) and systems (CTMS, eTMF, EDC, IXRS)
• Proven ability to build positive relationships with stakeholders
• Understanding of medical terminology and clinical trial activities

• interpersonal skills
• organizational skills
• client-focused communication
• MS Office
• MS Project
• PowerPoint

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