Senior Clinical Project Manager – Oncology

Overview

In this role you lead full-service clinical projects in oncology for global ph I–IV trials, ensuring delivery within scope, budget, and timelines. You will oversee cross-functional teams and client relationships to drive study success and quality. You work with both internal stakeholders and sponsors, shaping strategies from proposal through study completion. This is a high-energy, collaborative environment where you influence trial outcomes and contribute to precision medicine initiatives.

Pay / Benefits

• work-life balance
• collaborative environment
• growth and development opportunities
• team-oriented culture

Responsibilities

• Lead full-service clinical projects across global/regional ph I–IV oncology trials
• Oversee all functional departments to ensure timelines, cost, scope, and quality
• Serve as primary client liaison and lead proposal activities and presentations
• Manage study governance, budgets, and timelines; coordinate data management, safety, clinical, biostatistics, etc.
• Prepare status updates and define deliverables and performance metrics
• Review protocols and essential study documents (plans, consents, budgets)
• Contribute to cross-functional study teams and sponsor communications
• Drive quality and efficient trial execution through active team collaboration
• Possibly run international trials and manage client relationships end-to-end

Key requirements

• Previous full-service/global PM experience in CRO
• Extensive Clinical Operations background in CRO
• At least 4 years in a clinical trial PM role
• Experience managing oncology studies
• GCP/ICH knowledge and clinical development process understanding
• Ability to travel domestically and internationally
• Excellent English communication skills (written and spoken)
• Strong presentation skills
• Proficiency in MS Office, MS Project, PowerPoint and systems (CTMS, eTMF, EDC, IXRS)
• Ability to build positive internal and external relationships
• Solid understanding of medical terminology and clinical trial activities

• strong interpersonal skills
• excellent stakeholder management
• effective communicator
• CTMS
• eTMF
• EDC

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