Full Time

Clinical Trial Assistant

Sun Pharma
Mumbai
Salary Competitive
Posted 30/12/2025

About the Role

About the role & responsibilities
• Maintain study documents including protocols, ICFs, CRFs and reports
• Organize electronic and paper trial master files
• Coordinate meetings, travel arrangements and minutes
• Support regulatory document preparation and submissions
• Ensure compliance with GCP and regulatory standards
• Track site invoices and payments
• Manage vendor code generation and vendor tracking


Qualification
• Bachelor’s / Master’s in Pharmacy, Life Sciences, Biology, Chemistry, Nursing or Public Health
• PG Diploma in Clinical Research accepted


Experience
• 0–2 years
• Freshers eligible


Skills
• Clinical documentation management
• GCP and regulatory compliance knowledge
• MS Office proficiency
• Coordination and communication skills
• High attention to detail


About the company
• Sun Pharmaceutical Industries Ltd is India’s largest pharmaceutical company with global operations


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