Clinical Data Analyst II
This role supports clinical trial data review, cleaning, and query management, ensuring accurate data for regulatory submissions. The analyst will resolve data discrepancies, perform CRF freeze and lock activities, and coordinate with vendors and internal teams across multiple Indian sites.
Skills required
About this role
When our values align, there's no limit to what we can achieve.
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.
Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.
Job Summary
We are seeking a Clinical Data Management Associate with 4+ years of experience to support clinical trial data review, data cleaning, query management, and vendor data reconciliation activities. The role involves reviewing clinical data listings, resolving data discrepancies, performing CRF freeze and lock activities, coordinating with internal and external stakeholders, conducting User Acceptance Testing (UAT), and maintaining study documentation within Veeva Vault/eTMF. The ideal candidate will have hands-on experience with EDC systems, clinical data review tools, and a strong understanding of clinical research data management processes.
Skillsets
- Clinical Data Review and Data Cleaning
- Clinical Data Listings Review
- Query Management and Discrepancy Resolution
- Vendor Data Reconciliation, including Local Lab Review
- External Data Review and Reconciliation
- CRF Freeze and Lock Activities
- User Acceptance Testing (UAT) for Listings, Screens, and Edit Checks
- eTMF Documentation and Veeva Vault Management
- Clinical Data Workbench Experience
- Knowledge of Clinical Trial Data Management Processes
- Understanding of ICH-GCP, Regulatory Guidelines, and 21 CFR Part 11
- Cross-functional Collaboration and Stakeholder Management
- Strong Written and Verbal Communication Skills
Tools & Systems:
- EDC: Medidata RAVE (Preferred), Oracle Clinical
- Data Review: J-Review, Spotfire
- Documentation: Veeva Vault, eTMF
- Microsoft Office Suite, Microsoft Project, PowerPoint
Qualification
- Bachelor's degree in Life Sciences, Pharmacy, Biotechnology, Clinical Research, or a related scientific discipline.
- Minimum 4+ years of experience in Clinical Data Management within a CRO, pharmaceutical, or biotechnology environment.
- Hands-on experience with EDC systems, preferably Medidata RAVE and Oracle Clinical.
- Experience in data review, query management, vendor reconciliation, and database lock activities.
- Working knowledge of clinical research regulations, GCP guidelines, and clinical trial processes.
- Experience with Veeva Vault and eTMF documentation is preferred.
Location- Hybrid