Clinical Project Manager, Immuno-oncology, IQVIA Biotech

Key Responsibilities

• Lead the planning, execution, and delivery of clinical studies.
• Manage cross-functional project teams and drive achievement of study milestones.
• Serve as the primary point of contact for sponsors and key stakeholders.
• Monitor study progress, identify risks, and implement solutions proactively.
• Ensure compliance with protocols, regulatory requirements, and company processes.
• Manage project financials, forecasting, and scope changes.
• Support business development activities, including bid defenses and proposal strategy.
• Mentor team members and promote best practices across projects.

Qualifications

• Bachelor’s degree in Life Sciences or a related field.
• 7+ years of clinical research experience, including at least 4 years of project management experience.
• Strong knowledge of clinical trial conduct, ICH-GCP, and applicable regulatory requirements.
• Proven experience leading global or multi-regional clinical studies.
• Excellent leadership, communication, stakeholder management, and problem-solving skills.
• Strong financial and project management acumen.

Pay

The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.