Role & Responsibilities
• Independently manage multiple sites and complex clinical studies
• Lead site monitoring activities ensuring protocol, GCP, and regulatory compliance
• Review monitoring reports, SDV quality, and site performance metrics
• Support junior CRAs through mentoring and guidance
• Proactively identify risks and drive issue resolution and escalation
• Ensure inspection readiness and high-quality TMF maintenance
Qualification
• Graduate or Postgraduate in Life Sciences
• Pharmacy, Biotechnology, Nursing, or related disciplines
Experience
• 5–6 years of clinical research monitoring experience
Skills
• Strong expertise in ICH-GCP and global clinical trial regulations
• Leadership and stakeholder management skills
• Ability to manage complex studies independently
• Excellent analytical, communication, and documentation skills
About the Company
• Sanofi is a leading global healthcare company committed to advancing clinical research to deliver innovative therapies and improve patient outcomes worldwide
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