Clinical Data Associate

Role & responsibilities

• Assist in collecting, reviewing, and maintaining clinical trial data for accuracy and completeness.
• Perform clinical data entry and verification using Electronic Data Capture (EDC) systems.
• Identify missing, inconsistent, or incorrect data and assist in raising data queries.
• Support clinical data cleaning and discrepancy resolution as per study protocols.
• Maintain clinical trial documentation in accordance with Standard Operating Procedures (SOPs) and Good Clinical Practice (GCP) guidelines.
• Ensure data confidentiality and compliance with applicable clinical research requirements.
• Coordinate with clinical research teams to resolve data-related issues.
• Assist with database quality checks and routine data management activities.
• Maintain accurate records and meet assigned timelines while following quality standards.

Preferred candidate profile

• B.Pharm, M.Pharm, B.Sc., M.Sc., Biotechnology, Microbiology, Life Sciences, or other relevant healthcare qualifications.

• Basic computer skills, including MS Excel and MS Office.

• Strong attention to detail, analytical thinking, and data accuracy.