
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.
🔥 0 minutes ago
🏖️ New Jersey, North Carolina, +2 more states – Remote
💵 $93.1k - $285.5k / year
⏰ Full Time
🔴 Lead
👨⚕️ Medical Director
🦅 H1B Visa Sponsor
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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.
• Lead the Study Management Team and provide regular updates on trial deliverables. • Ensure real-time tracking and documentation of trial progress. • Maintain inspection-readiness throughout the trial lifecycle. • Act as the primary contact for country and regional staff and internal teams. • Partner with Global Trial Leads to oversee central trial activities from start-up to close-out. • Create and maintain trial-specific documents (e.g., Monitoring Guidelines, ICFs, Blinding Plans). • Establish country budgets and monitor actuals vs. forecast.
• Bachelor’s degree in Life Sciences (Biology, Chemistry, Biochemistry, Nursing, Pharmacy) or equivalent. • Minimum 8 years of experience, with proven leadership in complex trials at a large pharmaceutical company. • Strong knowledge of ICH-GCP and local regulatory requirements. • Proven ability to lead cross-functional teams and manage global trials. • Proficiency in Microsoft Office, CTMS, TMF, and other clinical systems. • Experience in virtual team coordination and stakeholder engagement.
• Health insurance • Retirement plans • Flexible work arrangements • Paid time off • Professional development • Bonuses
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