Senior Clinical Project Manager – Oncology

About the role

IQVIA Biotech is seeking an experienced CPM/Senior Clinical Project Manager to lead oncology clinical studies. The role involves overseeing study execution, managing cross‑functional teams and ensuring quality, speed and cost efficiency.

Key responsibilities

• Accountable for execution of clinical studies or assigned portions, optimizing speed, quality and cost.
• Set objectives for the core project team and assess performance.
• Develop integrated study management plans with the core team.
• Monitor progress against contract and communicate proactively to stakeholders.
• Manage risks, lead problem‑solving and implement corrective actions.
• Maintain financial success, forecast and identify acceleration opportunities.
• Build and lead cross‑functional project team and manage change control.
• Serve as primary contact with the customer and support business development.

Required profile

• Bachelor’s degree in life sciences or a related field.
• Minimum 5 years of relevant experience, including at least 1 year in project management.
• Advanced knowledge of clinical trial conduct and regulatory requirements (ICH GCP, local laws).
• Broad protocol and therapeutic area knowledge, especially oncology.
• Strong written and verbal communication skills in English.
• Ability to lead cross‑functional teams and mentor junior staff.
• Demonstrated decision‑making and results‑oriented approach.

Required skills

• ICH GCP
• Clinical trial conduct
• Project financial management
• Regulatory compliance
• Protocol development