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Hiring Clinical Data Management Analyst (EDC Programmer)
Syngene
Bangalore
1–2 Years
CDM / EDC
Clinical Research
🏢 About Company
Syngene International Ltd is a leading Contract Research, Development, and Manufacturing Organization (CRDMO) offering end-to-end services from drug discovery to development. It provides strong exposure to global clinical trials and advanced clinical data systems.
💼 Job Overview
- Role: Clinical Data Management Analyst (EDC Programmer)
- Department: Clinical Data Management
- Location: Bangalore
- Experience: 1–2 Years
- Type: Full-Time
📌 Key Responsibilities
Database Development:- Design & develop clinical study databases
- Build eCRFs, edit checks, and workflows
- Translate protocol into database specifications
- Perform UAT & database validation
- Develop test scripts and edit checks
- Ensure 21 CFR Part 11 compliance
- Handle data queries and cleaning activities
- Troubleshoot EDC system issues
- Implement mid-study updates
- Maintain audit trails & documentation
🎓 Eligibility
- Bachelor’s / Master’s in Computer Science / IT
- 1–2 years experience in EDC / CDM
💻 Required Skills
- EDC Tools: Medidata Rave / Veeva / Inform / Clinion
- Knowledge of CDISC standards
- Understanding of GCP guidelines
- Strong analytical & troubleshooting skills
- Experience in database build & validation
🚀 Career Growth
- Clinical Data Manager
- EDC Programmer
- Clinical Data Analyst
- Clinical Systems Specialist
🎯 Interview Tips
- Revise EDC systems (Rave, Inform basics)
- Understand eCRF design & edit checks
- Learn CDISC (SDTM basics)
- Prepare UAT & validation concepts
- Revise GCP & clinical trial lifecycle
📚 Helpful Resources:
📌 Note Before You Apply:
Hands-on EDC experience is key for this role. Candidates with Rave/Veeva exposure have higher chances.
Hands-on EDC experience is key for this role. Candidates with Rave/Veeva exposure have higher chances.
👇 Apply Here 👇
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