Role & Responsibilities
• Execute site monitoring activities in line with study protocol, SOPs, ICH-GCP, and regulatory requirements
• Conduct site initiation, routine monitoring, and close-out visits
• Perform source data verification (SDV) and ensure data accuracy and quality
• Ensure timely query resolution and compliance with study timelines
• Maintain essential documents and Trial Master File (TMF)
• Build and maintain strong relationships with investigators and site teams
Qualification
• Graduate or Postgraduate in Life Sciences
• Pharmacy, Biotechnology, Nursing, or related disciplines
Experience
• 1–3 years of experience as a Clinical Research Associate or similar role
Skills
• Strong knowledge of ICH-GCP and clinical trial processes
• Excellent communication and coordination skills
• Good documentation and reporting abilities
• Willingness to travel as per study requirements
About the Company
• Sanofi is a global biopharmaceutical company focused on transforming patient lives through innovative clinical research and development
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