Role & Responsibilities
• Independently manage multiple sites and complex clinical studies
• Lead site monitoring activities and ensure protocol and regulatory compliance
• Drive data quality, patient safety, and risk mitigation strategies
• Mentor and guide junior CRAs
• Support audits, inspections, and cross-functional collaboration
Qualification
• Life Sciences graduate/postgraduate
Experience
• 5-6 years of experience as a Clinical Research Associate (CRA)
• Extensive CRA experience, with a strong expertise in GCP, regulatory guidelines, and monitoring best practices
• Proven ability to manage sites independently and handle escalations
Skills
• Strong communication, coordination, and documentation skills
• Excellent leadership, stakeholder management, and problem-solving skills
About The Company
• Sanofi Careers - Leading global healthcare company providing medicines and treatments across diverse therapeutic areas
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