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 managing study execution, ensuring quality, timelines, and cost efficiency while collaborating with cross‑functional teams and customers.

Key responsibilities

• Execute clinical studies or assigned portions, optimizing speed, quality and cost while adhering to study tools, training materials and standard processes.
• Set objectives for the core project team, communicate performance, and monitor progress against contract commitments.
• Develop integrated study management plans and collaborate with functional groups to achieve milestones and resolve issues.
• Manage risks, contingencies and problem‑solving efforts, ensuring corrective and preventive actions are implemented.
• Maintain financial success of the project, forecast revenue opportunities and control scope changes.
• Build and lead cross‑functional teams, acting as primary contact with customers and supporting staff development.

Required profile

• Bachelor’s degree in life sciences or a related field.
• At least 5 years of relevant experience, including more than 1 year of project management experience.
• Strong understanding of clinical trial conduct, ICH GCP and local regulatory requirements.
• Experience managing project financials, contractual obligations and change control.
• Excellent written and verbal communication skills in English and strong customer‑service orientation.

Required skills

• Knowledge of ICH GCP and clinical research regulatory frameworks.
• Broad protocol knowledge with therapeutic expertise in oncology (cardiovascular, metabolic, renal, obesity knowledge considered a plus).
• Proficiency with standard clinical project management tools and general computer software.
• Ability to analyze data, make decisions and drive results across geographies.