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Quadrangle is hiring an experienced Clinical Database Programmer for a full-time role in Gurugram. This is an excellent career opportunity for professionals with strong experience in clinical data management, EDC systems, CDASH standards, and database design in clinical trials.
If you have hands-on exposure to oncology, cardiology, neurology, or medical device studies — this role could be the perfect next step in your career growth.
🔍 Key Responsibilities
As a Clinical Database Programmer, your responsibilities will include:
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- Reviewing functional requirement documents from clinical project teams.
- Developing, validating, and maintaining eCRFs and related EDC modules.
- Creating standard CDASH-compliant CRF libraries.
- Implementing edit check specifications and quality control checks per study protocol.
- Performing mid-study database updates based on approved change requests.
- Providing annotated and blank CRFs to stakeholders.
- Updating SOPs in alignment with regulatory changes.
- Managing user/site administration including roles, access, and permissions.
- Ensuring secure database access and compliance.
- Performing database testing and maintaining audit-ready documentation.
- Collaborating with the EDC product support team for troubleshooting and enhancements.
🎓 Required Qualifications
- Education: B.Pharm, M.Pharm, B.Tech/M.Tech (Biotechnology/Bioinformatics/Biomedical Engineering/Computer Science) or equivalent.
- Experience: Minimum 3 years in clinical data management with 1–2 years in database design.
- Strong knowledge of EDC systems (Zelta platform highly preferred, Veeva EDC desirable).
- Familiarity with CDASH and SDTM standards.
- Experience with Power BI or other data visualization tools is a plus.
- Preferred experience in Oncology, Hematology, Neurology, Cardiology, or medical device studies.
⭐ Preferred Skills
- Zelta (formerly IBM/Merative Clinical Development) certification
- Knowledge of Endpoint Adjudication, Data Migrator, Smart Report, and Inventory modules
- Strong understanding of database structure, edit checks, and clinical protocol requirements
💼 Benefits & Growth Opportunities
- Competitive compensation package (₹13–15 LPA based on experience)
- Exposure to global clinical trials and regulatory workflows
- Opportunity to work with leading experts in clinical data management
- Skill development in advanced EDC platforms and medical device studies
📍 Job Location
📌 Gurugram, Haryana — India
(Full-time, permanent role)
📝 How to Apply
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