Senior Clinical Project Manager – Oncology (CPM)

About the role

IQVIA Biotech is seeking an experienced CPM/Senior Clinical Project Manager to lead oncology clinical trials. The role requires at least four years of regional or global CPM experience and a strong background in oncology studies.

Key responsibilities

• Execute clinical studies or study portions, optimizing speed, quality and cost while ensuring compliance with study tools, training materials and standard processes.
• Set objectives for the core project team, communicate performance, and monitor progress against contracts.
• Develop integrated study management plans and collaborate with functional groups to achieve milestones and resolve issues.
• Manage risks, lead problem‑solving, and implement corrective and preventive actions to maintain project quality.
• Maintain the financial health of the project, forecast revenue opportunities and control scope changes.

Required profile

• Bachelor’s degree in life sciences or related field.
• Minimum 5 years of relevant experience, including at least 1 year in project management.
• Deep knowledge of clinical trial conduct and regulatory requirements such as ICH GCP.
• Experience managing project financials and contractual obligations.
• Strong written and verbal communication skills in English.

Required skills

• ICH GCP and other clinical research regulatory knowledge.
• Clinical trial management and protocol execution.
• Project financial management.
• Proficiency with standard software tools (e.g., Microsoft Office).