Senior Clinical Data Associate

About the role

Clinical Data Management team at Precision Medicine Group supports end‑to‑end clinical trial data processes from study start‑up to post‑database lock. The Senior Clinical Data Associate backs the Lead DM, builds and tests databases, performs data entry, quality control, medical coding, and trains staff on CRF/EDC tools. Bangalore, Karnataka, India – on‑site work model.

What you’ll do

• Support Lead DM and ensure timely data management tasks
• Build and test clinical databases and conduct UAT
• Perform data entry, quality control, and medical coding
• Develop CRF specifications and train research personnel
• Coordinate with sponsors, vendors, and project teams
• Generate status and metric reports
• Assist with SAS programming and SOP documentation
• Present software demos and training sessions

What you’ll bring

• 5+ years experience
• Proficiency in Microsoft Office (Word, Excel, PowerPoint, Outlook)
• Professional English communication
• Basic knowledge of drug/device/biologic development
• Medical coding (MedDRA, WHODrug)
• Understanding of CDISC standards (CDASH, SDTM, ADaM)

Nice to have

• 5+ years experience
• Proficiency in Microsoft Office
• Professional English communication
• Basic knowledge of drug/device/biologic development
• Medical coding (MedDRA, WHODrug)
• Understanding of CDISC standards

Skills

Education

Bachelors