Overview
Clinical Data Analyst II to support data review, data cleaning, study build, vendor reconciliations, and database lock processes across global clinical trials.
What you'll do
- Review clinical data listings and manage data discrepancies.
- Support CRF and edit check development.
- Conduct UAT activities during study build and validation phases.
- Review complex external data sources.
- Ensure compliance with GCP and regulatory requirements.
- Collaborate cross-functionally and mentor junior CDM staff.
What you'll need
- Minimum 4+ years of clinical data management experience.
- Minimum 4+ years of experience in clinical data review and clinical data management.
- Hands-on experience with Medidata RAVE and other EDC systems.
- Experience supporting study build activities including CRF design, edit checks, and integrations.
- Experience performing UAT during study build and validation phases.
- Strong experience in vendor reconciliation and external data review.
- Knowledge of ICH-GCP guidelines, regulatory requirements, and clinical trial processes.
- Experience working within Veeva Vault and eTMF environments.
Nice to have
- Experience in Oncology, Hematology, Cardiovascular, Fibrosis, and/or Cell Therapy studies preferred.
- CCDM Certification is advantageous.
- Stable employment history with tenure of at least one year with previous employers or valid explanation for transitions.
Details
- Location: India - Hyderabad.
Read the full description and apply on the company’s own careers page.
