Clinical Project Manager

As a Clinical Project Manager at IQVIA, you will lead delivery of clinical studies, ensuring they meet contractual, quality, and regulatory standards. You will work with cross-functional teams to optimize speed, cost, and study quality, while managing risks and maintaining stakeholder communications. The role focuses on delivering value through therapeutic expertise and IQVIA solutions to drive operational excellence. You will build and mentor project teams, coordinate vendors, and contribute to financial performance and customer satisfaction. This is an opportunity to shape trial delivery in a collaborative, global environment and to advance patient outcomes through efficient study delivery

• Deliver and manage smaller, local studies with integrated study plans
• Execute clinical studies per contract, optimizing speed, quality and cost; ensure standard processes and training are followed
• Set objectives for core project teams and assess performance
• Collaborate with cross-functional groups to meet milestones and resolve issues
• Monitor progress and proactively report to stakeholders; manage risks and contingencies
• Ensure project quality by addressing risks and implementing CAPAs
• Serve as primary or backup customer contact and coordinate with IQVIA stakeholders
• Build and lead cross-functional project teams to achieve milestones and manage obstacles
• Ensure financial success of projects and identify opportunities to accelerate revenue
• Oversee vendor management as needed and support staff development and mentorship

• Bachelor's Degree Life sciences or related field
• 3+ years as Project Manager and 5+ years of clinical research experience
• Knowledge of clinical trial conduct and regulatory requirements (ICH GCP and local laws)
• Strong written and verbal communication in Dutch and English
• Strong problem-solving, decision-making, and prioritization skills
• Attention to detail and results-oriented work approach
• Proficiency with MS Office (Word, Excel, PowerPoint)
• Ability to work across geographies and understand cultural differences
• Understanding of project financials and contractual obligations
• Willingness to work at Sponsor's office in Haarlem at least 2 days/week
• Location-based eligibility per sponsor requirements

• Strong communication skills
• Problem solving
• Decision making with clarity
• MS Office proficiency (Word, Excel, PowerPoint)
• Knowledge of clinical trial regulatory requirements (ICH GCP)
• Vendor management