
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.
🕒 July 28
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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.
• Perform feasibility, site activation and maintenance activities for investigative sites in assigned studies • Work according to applicable regulations, SOPs, work instructions, project requirements and contractual/budgetary guidelines • Work closely with the Site Activation Manager, Project Management team and other departments • Review site documents for completeness, consistency and accuracy • Prepare site documents and distribute completed documents to sites and internal project team members • Inform team members when regulatory, contractual and other site documents are complete • Update and maintain internal systems, databases, tracking tools, timelines and project plans • Review, track and follow up on questionnaires, CDAs, regulatory and ethics documents, Informed Consent Forms and Investigator Pack release documents
• Bachelor's Degree Life science or related field • 2 years’ experience in a clinical research environment • Previous experience in regulatory or contract negotiation • Advanced level of English is mandatory • CV must be submitted in English
• Home based role / work from home
Apply Now🕒 July 28
Salesperson handling tele-parts sales via phone at Grupo IESA. Responsible for client prospecting, order issuance, and follow-up on orders.
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🕒 July 27
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🕒 July 25
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🕒 July 24
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