IQVIA
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.
Global Trial Manager, Late Phase Studies
🔥 1 hour ago
📊 Check your resume score for this job
Improve your chances of getting an interview by checking your resume score before you apply.
IQVIA
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 critical aspects of global studies and collaborate across functions to drive success • Draft sections of protocols, CRFs, training materials, and data review plans • Oversee data review and TMF audit readiness • Forecast/manage investigational product supply • Support study closeout, issue resolution, and lifecycle budget tracking • Coordinate CRO/vendor selection and performance • Facilitate advisory boards (DMCs/Steering Committees) and serve as the site liaison
🎯 Requirements
• Advanced degree in life sciences or healthcare • 2–5 years' global experience managing phase IV, PASS, PAES, or NIS trials • Strong track record in protocol development, study startup, and regulatory writing (e.g. PSURs, DSURs, NDA/BLA reports) • Excellent communication, organizational, and collaboration skills • Deep understanding of GCP and clinical trial design • Passion for advancing real-world evidence and patient outcomes
🏖️ Benefits
• Competitive salary • Work from home options • Professional development opportunities • Zero tolerance policy for candidate fraud
Apply NowSimilar Jobs
🕒 2 days ago
Responsable de Incidencia Pública y Ecosistema en Legados, liderando iniciativas estratégicas y relaciones institucionales para influir en la agenda pública española. Rol senior enfocado en construir alianzas y ejecución de proyectos.
🗣️🇪🇸 Spanish Required
🕒 July 2
Manager overseeing Commercial Quality operations for Ergomed, a pharmacovigilance service provider. Leading compliance with GxP regulations and supporting business development processes.
🕒 July 2
Manager Clinical Operations at Thermo Fisher Scientific overseeing and developing clinical operations teams. Responsible for performance management, training, and operational excellence in global clinical trials.
🕒 July 1
Proposals Manager responsible for leading proposal development in pharmacovigilance sector globally. Ensuring quality proposals while collaborating with departments and managing budgets.
🕒 June 30
Supplier Manager handling WorkMotion’s global Employer of Record network. Facilitating partner relationships and ensuring compliance in managing international teams.
