Clinical Project Manager - Global Study Leadership

About the role

IQVIA's Global Study Leadership team delivers clinical trials through therapeutically aligned and customer-dedicated delivery models, covering a wide portfolio of studies in Oncology, Rare Disease, CNS, Cardiovascular, Immunology, Respiratory, Cell & Gene Therapy, Infectious Disease, Ophthalmology and Women's Health. As a Clinical Project Manager you will lead regional and global clinical studies or study workstreams, partnering with sponsors and cross-functional teams to deliver studies efficiently, compliantly and with a focus on quality, timelines and patient impact.

Key responsibilities

• Lead the delivery of regional and global clinical studies or study workstreams from start-up through close-out
• Build strong relationships with sponsors as a primary or key project contact and ensure an exceptional customer experience
• Lead and coordinate cross-functional teams to achieve milestones and study objectives
• Develop and execute study management plans
• Manage timelines, budgets, quality, risks and operational performance throughout the project lifecycle
• Drive proactive issue resolution, risk mitigation and stakeholder alignment
• Support financial oversight, forecasting, change control and vendor management where applicable
• Ensure compliance with ICH-GCP, regulatory requirements, SOPs and contractual commitments
• Contribute to continuous improvement through lessons learned, best practice sharing and supporting developing team members

Required profile

• Bachelor's degree in Life Sciences, Healthcare or a related scientific discipline
• 5+ years of clinical research experience, including project management in a CRO, pharmaceutical or biotechnology environment
• Experience leading clinical studies, study workstreams or cross-functional project teams
• Proven ability to manage timelines, risks, quality, budgets and operational performance
• Experience building sponsor and stakeholder relationships in a global environment

Required skills

• Strong knowledge of clinical trial conduct, ICH-GCP guidelines and applicable regulatory requirements
• Strong communication, collaboration, problem-solving and decision-making skills
• Ability to thrive in a fast-paced, matrixed environment while balancing multiple priorities