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Indero Hiring Clinical Study Builder | Remote Job India
🏢 Indero
🌍 Remote (India)
⏳ 2+ Years
💰 ₹6 – ₹12 LPA
Looking for a remote clinical data management job? Indero is hiring a Clinical Study Builder for India. This role is ideal for professionals with experience in Veeva CDMS, eCRF design, and clinical database systems.
📋 Job Overview
- Role: Clinical Study Builder
- Company: Indero (Global CRO)
- Location: Remote (India)
- Experience: Minimum 2 Years
- Industry: Clinical Data Management / CDMS
📌 Key Responsibilities
- Design eCRFs based on study protocols
- Configure Veeva CDMS (edit checks, derivations)
- Build databases in Medrio & Medidata Rave
- Perform UAT testing & validation
- Support deployment & training
- Collaborate with Data Managers & Statisticians
- Ensure compliance with GCP & ICH guidelines
🎓 Eligibility
- B.Sc / M.Sc Life Sciences
- Minimum 2 years CDMS / Study Build experience
- Veeva Study Builder experience required
💻 Required Skills
- Veeva CDMS / Medidata Rave / Medrio
- eCRF design & database programming
- Clinical trial workflow understanding
- Strong problem-solving & communication
🚀 Career Growth
- Clinical Data Manager
- CDMS Specialist
- Clinical SAS Programmer
- Clinical Data vs SAS Guide
💡 Interview Tips
- Prepare Veeva CDMS concepts
- Revise CRF design & validation
- Practice Quiz
📄 Resume Tips
- Highlight CDMS tools (Veeva, Rave, Medrio)
- Add project-based experience
- Use keywords: eCRF, UAT, Data Validation
- CDISC Guide
📌 Tip: Remote CDMS roles are high-demand — apply early.
🚀 Job Application Link
📌 Important Note Before You Apply:
Kindly read the full job description carefully before applying. Ensure your profile aligns with clinical database design, EDC (Electronic Data Capture) study building, CRF/eCRF development, data validation specifications, and clinical trial software configuration workflows before proceeding.
Kindly read the full job description carefully before applying. Ensure your profile aligns with clinical database design, EDC (Electronic Data Capture) study building, CRF/eCRF development, data validation specifications, and clinical trial software configuration workflows before proceeding.
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