Assist in the design, development, and testing of data collection tools (e.g., Case Report Forms/eCRFs).
Perform data entry and data validation activities in clinical trial databases.
Assist in query management and data cleaning activities under supervision.
Support database lock and archiving activities.
Participate in study team meetings and training sessions.
Ensure compliance with Good Clinical Practice (GCP), Standard Operating Procedures (SOPs), and regulatory guidelines.
Maintain documentation and audit trails as per organizational requirements.
Job Types: Full-time, Permanent, Fresher
Pay: ?295,874.55 - ?626,810.42 per year
Benefits:
Health insurance
Paid sick time
Provident Fund
Work Location: In person
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