Trial Delivery Manager, Sponsor Dedicated (Remote)

About the role

iQVIA is seeking a Senior Project Lead / Associate Director, Clinical Trial Management to provide centralized, global clinical trial oversight within its Functional Service Provider (FSP) model. The role partners with Global Trial Leadership and cross-functional stakeholders to plan, execute and deliver complex clinical trials across regions and vendors. It is a home-based remote role on the East Coast, leading Study Management Teams and overseeing country and site-facing activities from start-up through close-out.

Key responsibilities

• Lead and coordinate global and regional clinical trial management for internally managed and outsourced studies, acting as primary point of contact for country, regional and functional stakeholders.
• Drive trial delivery across the full lifecycle, keeping milestones, timelines and deliverables clear, and act as central subject matter expert for assigned protocols.
• Oversee CROs and global vendors (IWRS/IVRS, central laboratory, ePRO/eCOA, imaging, translation, ancillary supplies, investigator meetings), approving deliverables, invoices and spend.
• Maintain inspection readiness under ICH-GCP, lead CAPA work and support Health Authority inspections and audits.
• Manage feasibility, regional enrollment commitments and recruitment plans, and proactively identify and escalate risks.
• Oversee documentation, filing, archiving and retention, including Monitoring Guidelines, informed consent forms, IMP and blinding documentation, and support database lock.
• Lead teams, coach less experienced members and contribute to process improvements.

Required profile

• Bachelor's degree (or equivalent) in Life Sciences (e.g. Biology, Chemistry, Nursing, Pharmacy).
• Base level: 6+ years of clinical trial management experience in pharma and/or CRO environments; Advanced level: 8+ years, including leadership of complex global studies.
• Proven experience managing trials from start-up through database lock and close-out.
• Experience coordinating global, virtual teams in a large matrix environment for 2-3+ years.
• Therapeutic area experience required; fluent in English, with local language proficiency as required; willingness to travel as needed.

Required skills

• Deep knowledge of ICH-GCP, regulatory requirements and clinical operations best practices.
• Project management, planning and risk mitigation; ability to manage country and vendor budgets.
• Experience with CTMS, TMF systems and Microsoft applications; monitoring experience preferred.

The potential base pay range is $93,100-$295,500 per year, depending on qualifications, location and schedule; incentives, bonuses and benefits may also apply.