
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.
🔥 0 minutes ago
🇨🇦 Canada – Remote
💵 $74.7k - $124.5k / year
⏰ Full Time
🟢 Junior
🟡 Mid-level
🧪 Clinical Research
👻 Ghost score 0%
🗣️🇫🇷 French Required
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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.
• Monitor Phase I–IV clinical trials for compliance with protocols, GCP/ICH guidelines, and regulatory requirements • Manage site activities from start-up through close-out • Conduct site selection, initiation, monitoring, and close-out visits • Train site personnel on study protocols, EDC systems, and study requirements • Ensure high-quality source documentation and data integrity • Resolve queries in a timely manner • Oversee investigational product accountability and regulatory document collection • Serve as the primary site contact and maintain regular communication • Prepare monitoring reports according to SOPs and timelines • Support investigator meetings and collaborate with CTMs/Lead CRAs
• Bilingual in French and English (required) • Bachelor's degree required, preferably in life sciences or a related discipline • An equivalent combination of education, training, and experience may be accepted in lieu of a degree • At least 1 year of on-site monitoring experience required • Ability to travel 65–70% • Knowledge of clinical trial protocols, GCP/ICH guidelines, and regulatory requirements • Experience with oncology monitoring • Experience with EDC systems
• Incentive plans, bonuses, and/or other forms of compensation may be offered • Health and wellness benefits • Other benefits • Equal opportunity employer • Accommodations for applicants with disabilities throughout the recruitment process
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