Clinical Trial Assistant
About the Role
Roles & Responsibilities
• Maintain clinical trial documents such as protocols, ICFs, CRFs, and study reports
• Organize and manage electronic and paper-based study files
• Schedule meetings, prepare MOMs, and provide administrative support
• Assist in preparation and submission of documents to Ethics Committees and regulatory authorities
• Support GCP compliance and regulatory requirements
• Coordinate site-related activities including invoice tracking and payments
• Perform vendor code generation and maintain vendor records
Qualification
• B.Pharm / M.Pharm
• Life Sciences / Biology / Chemistry
• Nursing / Public Health
• PG Diploma in Clinical Research
Experience
• 0–2 years in Clinical Research
• Freshers can apply
Skills
• Knowledge of GCP and clinical trial documentation
• Good organizational and coordination skills
• Attention to detail and compliance mindset
• Proficiency in MS Office tools
About the Organization
Sun Pharmaceutical Industries Ltd. is India’s leading pharmaceutical company with a strong global presence across specialty and generic medicines. The company is known for its high standards in research, quality, and regulatory compliance. Sun Pharma offers a dynamic work environment with excellent learning and long-term career growth opportunities.
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