Clinical Trial Assistant
About the Role
Role & Responsibilities
• Maintain study documentation including protocols, ICFs, CRFs and clinical reports
• Organize and manage electronic and paper study files
• Support meeting scheduling, minutes preparation and travel coordination
• Assist in preparation and submission of regulatory documents
• Support GCP compliance and regulatory requirements
• Track site invoices and payment status
• Handle vendor code generation and vendor tracking
• Support site coordination and communication activities
Qualification
• Bachelor’s or Master’s degree in Life Sciences / Pharmacy / Nursing / Public Health / Related discipline
• PG Diploma in Clinical Research (preferred)
Experience
• 0–2 years in Clinical Research
• Freshers are eligible
Skills
• Basic understanding of GCP and clinical research documentation
• Good organizational and coordination skills
• Strong documentation and communication abilities
• Proficiency in MS Office
About the Company
Sun Pharma is India’s largest pharmaceutical company and a global leader in specialty generics and innovative medicines.
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