
10,000+ employees
💼 Consulting
🏭 Manufacturing
📣 Marketing
💰 $1G Post-IPO Debt on 2023-05
Consulting • Manufacturing • 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.
🔥 1 hour ago
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10,000+ employees
💼 Consulting
🏭 Manufacturing
📣 Marketing
💰 $1G Post-IPO Debt on 2023-05
Consulting • Manufacturing • 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.
• Under general supervision, perform feasibility, site activation and some maintenance activities in assigned studies for investigative sites, according to applicable regulations, SOPs and work instructions, working closely with the Site Activation Manager (SAM), Project Management team, and other departments as necessary. • Review documents for completeness, consistency and accuracy, under guidance of senior staff. • Prepare site documents, reviewing for completeness and accuracy. • Inform team members of completion of regulatory contractual and other documents for individual sites. • Distribute completed documents to sites and internal project team members. • Support the updating and maintenance of internal systems, databases, tracking tools, timelines and project plans with accurate and complete project specific information. • Review, track and follow up the progress, the approval and execution of required documents such as questionnaires, CDAs, regulatory, ethics, Informed Consent Form (ICF) and Investigator Pack (IP) release documents.
• Bachelor's Degree Life science or related field. • With 2 years’ experience in a clinical research environment, with previous experience in regulatory or contract negotiation. • Advanced level of English is mandatory, you'll be in touch with sites from North America. • Please, submit your CV in English, it will be reviewed by a global team.
• Home based role
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