Associate Director Senior Study Lead - Single Sponsor Dedicated (home-based)

IQVIA is a leading global provider of clinical research services, dedicated to accelerating the development of innovative medical treatments. We are currently seeking an Associate Director Senior Study Lead to join our team in a fully remote capacity, where you will lead cross-functional clinical trial teams and guide the end-to-end management of complex clinical studies.

Key responsibilities

• Lead the planning, execution, and delivery of clinical studies while acting as the product owner for the clinical trial team.
• Promote operational excellence in the development of global clinical study protocols, reports, and essential study documentation.
• Implement proactive operational planning with effective contingency strategies and a strong risk management mindset.
• Manage study budgets and resource allocation to ensure cost-effective and high-quality project delivery.
• Foster a collaborative and psychologically safe environment within a global matrix organization.

Requirements

• Bachelor’s degree in life sciences or a healthcare-related field; an advanced degree is strongly preferred.
• At least 4 years of recent experience in clinical research or drug development across Phases I through IV.
• Minimum 3 years of experience in conducting complex clinical studies within a global pharmaceutical or CRO environment.
• Expert knowledge of international standards including GCP, ICH, and requirements from health authorities like the FDA and EMA.
• Proven ability to lead virtual teams and build effective relationships with diverse internal and external stakeholders.

What we offer

• The opportunity to work in a fully remote environment for a global leader in clinical research.
• Engagement in high-priority, complex clinical trials that directly impact patient outcomes.
• Professional development within a supportive, matrix-based organizational structure.