Senior Site Activation Coordinator, North America

🕒 September 15

🌐 Brazil, Argentina – Remote

🇧🇷 Brazil – Remote 🇦🇷 Argentina – Remote

⏰ Full Time

🟠 Senior

👻 Ghost score 20%

What it means: the chance that no one is really hiring for this job.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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IQVIA

WebsiteLinkedInAll Job Openings

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.

📋 Description

• Perform feasibility, site activation, and maintenance activities for investigative sites • Work according to applicable regulations, SOPs, work instructions, project requirements, and contractual/budgetary guidelines • Collaborate with the Site Activation Manager, Project Management team, and other departments • Review site documents for completeness, consistency, and accuracy • Prepare site documents and inform team members when regulatory, contractual, and other documents are complete • Distribute completed documents to sites and internal project team members • 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 • Support site activation activities at a country/region level under general supervision

🎯 Requirements

• Bachelor's Degree in Life Science or related field • 2 years’ experience in a CRO or over 4 years of experience at a site • Previous experience in regulatory/site activation tasks • Advanced level of English is mandatory • CV must be submitted in English • Ability to work with sites from North America • Knowledge of applicable local and/or international regulations, SOPs, project requirements, and contractual/budgetary guidelines

🏖️ Benefits

• Home based role • Global team collaboration • Opportunity to work in clinical research, commercial insights, and healthcare intelligence supporting life sciences and healthcare industries

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