
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.
🕒 September 25
Where this job comes from
Posted on IQVIA's careers page, not through a job board
First seen by Remote Rocketship September 25
Still open on IQVIA's site. Checked 7 hours ago.

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.
• Execute feasibility, site identification, regulatory, and start-up activities at the regional or country level • Serve as the Single Point of Contact for feasibility and site activation activities at investigative sites • Work closely with the Site Activation Manager, Project Management team, and other departments • Prepare, review, distribute, and manage site documents • Inform team members about completion of regulatory, contractual, and other site documents • 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 • Maintain site documentation, contracts, site performance metrics, project timelines, and site activation activities
• Bachelor's Degree in Life Sciences or a related field • At least 1 year of clinical research experience • Advanced level of English • Ability to work with North American sites • CV must be submitted in English
• Full-time employment
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