Trial Delivery Manager – Multi TA

🔥 1 hour ago

🏖️ New Jersey, North Carolina, +2 more states – Remote

🏖️ New Jersey – Remote 🌲 North Carolina – Remote 🍂 Massachusetts – Remote 🔔 Pennsylvania – Remote

💵 $93.1k - $285.5k / year

⏰ Full Time

🟡 Mid-level

🟠 Senior

👔 Manager

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IQVIA

WebsiteLinkedInAll Job Openings

10,000+ employees

⚕️ Healthcare Insurance

🧬 Biotechnology

🤖 Artificial Intelligence

💰 $1G Post-IPO Debt on 2023-05

Healthcare Insurance • Biotechnology • Artificial Intelligence

IQVIA is a global leader in data analytics and technology solutions, dedicated to improving health outcomes. The company utilizes its Connected Intelligence platform to harness the power of advanced data analytics and artificial intelligence, facilitating innovation in healthcare. IQVIA focuses on various areas, including clinical research, technology, and consulting services to solve complex healthcare challenges and accelerate the delivery of new therapies to patients.

📋 Description

• Lead and coordinate global and regional clinical trial management activities for internally managed and outsourced studies • Drive trial delivery across the full lifecycle: feasibility, site selection, startup, execution, and close-out • Act as primary point of contact for country, regional, and functional stakeholders within Clinical Development Operations • Provide oversight of CROs and global vendors supporting site-facing activities • Ensure continuous inspection readiness in accordance with ICH-GCP, applicable regulations, and sponsor SOPs • Lead feasibility activities and provide data-driven recommendations • Oversee trial documentation, filing, archiving, and retention • Provide coaching and mentoring to less experienced team members

🎯 Requirements

• Bachelor’s degree (or equivalent) in Life Sciences (e.g., Biology, Chemistry, Nursing, Pharmacy) • 6+ years of clinical trial management experience in pharma and/or CRO environments • 8+ years of clinical trial management experience, 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 • Deep knowledge of ICH-GCP, regulatory requirements, and clinical operations best practices • Strong project management, planning, and risk mitigation skills • Demonstrated ability to manage country and vendor budgets, including OOPs and cost drivers • Experience with CTMS, TMF systems, and Microsoft applications • Monitoring experience preferred (or equivalent central monitoring/data management experience) • Strong analytical, decision-making, and communication skills • Fluent in English; local language proficiency as required • Willingness to travel as needed.

🏖️ Benefits

• Health insurance • 401(k) matching • Paid time off • Professional development opportunities