Full Time
Clinical Trial Specialist
TRDFIN Support Services
Bengaluru
Competitive
Posted 30/12/2025
About the Role
About Role & Responsibilities
• Manage clinical trial documentation
• Perform clinical data analysis and reporting
• Ensure protocol compliance
• Support audits and inspections
Qualification
B.Pharm / M.Pharm / Pharm.D / MSc / BSc
Experience
0–3 years
Skills
• Clinical data management
• Documentation
• MS Excel & reporting
About the Company
TRDFIN provides clinical research and data management services to pharma companies
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