- Learn ICH guidelines, 21 CFR Part 11, ISO 9001 and ISO 7001.
- Gain exposure to eCRFs, CRF Completion Guidelines, Edit check specs, and DMP
- Contribute to study tracking and metric reports for use by the study team
- Contribute to user acceptance testing (UAT) of EDC and integrated systems including execution of test plan and scripts.
- Member of project team.
Job Requirements
- Bachelor's Degree in a scientific, medical, or clinical discipline or related field is required; Master's or PhD preferred
- 1-2 years of previous experience in clinical data management
- Hands-on experience with clinical trials and pharmaceutical development preferred
- Experience in the pharmaceutical or CRO industry must
- Experience with query and discrepancy management required
- Has a solid attention to detail
Disclaimer: This job posting and location has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.
📌 Clinical Data Associate (Bengaluru)
🏢 MMSH Clinical Research
📍 Bengaluru
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