Senior Clinical Project Manager (Respiratory, Ophthalmology, Immunology, Dermatology)

About the role

IQVIA is recruiting a Senior Clinical Project Manager to lead global clinical studies in Respiratory, Ophthalmology, Immunology and Dermatology. As the strategic leader of the studies, you will be accountable for delivering complex global clinical trials from start-up through close-out, ensuring quality, timeline, budget, regulatory and customer objectives are met. The role sits within Global Study Leadership, a global team that partners directly with pharmaceutical and biotechnology sponsors.

Key responsibilities

• Lead the delivery of complex global and multi-regional clinical studies, driving operational excellence and successful study outcomes.
• Serve as the primary strategic partner for sponsors, providing leadership, guidance and innovative solutions.
• Provide leadership and direction to cross-functional teams across regions, fostering collaboration and high performance.
• Oversee study timelines, budgets, quality, risks, financial performance and operational delivery.
• Drive proactive risk management, issue resolution, decision-making and stakeholder alignment throughout the study lifecycle.
• Ensure studies are delivered in compliance with ICH-GCP, regulatory requirements and contractual commitments.

Required profile

• Bachelor's degree in Life Sciences, Healthcare or a related scientific discipline.
• 7+ years of clinical research experience, including significant project management experience leading global or multi-regional clinical trials within a CRO, pharmaceutical or biotechnology environment.
• Experience leading Immunology, Dermatology, Respiratory, Ophthalmology global clinical studies is strongly preferred.
• Proven success leading cross-functional teams and managing study delivery, including timelines, budgets, quality, risks and operational performance.
• Demonstrated ability to build trusted sponsor relationships and manage senior stakeholders in a global environment.

Required skills

• Strong knowledge of clinical trial conduct, ICH-GCP guidelines and applicable regulatory requirements.
• Exceptional leadership, communication, problem-solving and decision-making skills.