
10,000+ employees
đŒ Consulting
đ Manufacturing
đŁ Marketing
đ° $1G Post-IPO Debt on 2023-05
Consulting âą Manufacturing âą Marketing
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.
đ„ 13 hours ago
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10,000+ employees
đŒ Consulting
đ Manufacturing
đŁ Marketing
đ° $1G Post-IPO Debt on 2023-05
Consulting âą Manufacturing âą Marketing
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.
âą Perform feasibility, site activation, and maintenance activities for investigative sites âą Work according to applicable regulations, SOPs, work instructions, project requirements, and contractual/budgetary guidelines âą Collaborate with the Site Activation Manager, Project Management team, and other departments âą Review site documents for completeness, consistency, and accuracy âą Prepare site documents and inform team members when regulatory, contractual, and other documents are complete âą Distribute completed documents to sites and internal project team members âą Update and maintain internal systems, databases, tracking tools, timelines, and project plans âą Review, track, and follow up on questionnaires, CDAs, regulatory and ethics documents, Informed Consent Forms, and Investigator Pack release documents âą Support site activation activities at a country/region level under general supervision
âą Bachelor's Degree in Life Science or related field âą 2 yearsâ experience in a CRO or over 4 years of experience at a site âą Previous experience in regulatory/site activation tasks âą Advanced level of English is mandatory âą CV must be submitted in English âą Ability to work with sites from North America âą Knowledge of applicable local and/or international regulations, SOPs, project requirements, and contractual/budgetary guidelines
âą Home based role âą Global team collaboration âą Opportunity to work in clinical research, commercial insights, and healthcare intelligence supporting life sciences and healthcare industries
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