Clinical Data Analyst I

Parexel International; Hyderabad; On-site; INR 800,000 - 1,200,000; Full time

Job summary

Parexel International is seeking a Clinical Data Analyst in Hyderabad with 2+ years of experience to support data review, cleaning, and query management for clinical trials. The role includes vendor data reconciliation, CRF freeze/lock activities, and UAT coordination with internal and external stakeholders.

Proficiency in EDC systems and data management processes is essential. Ideal candidates will have hands-on experience with Medidata RAVE and Oracle Clinical, and familiarity with Veeva

Qualifications

• Bachelor's degree in Life Sciences, Pharmacy, Biotechnology, Clinical Research, or a related scientific discipline.
• Minimum 2+ 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.

Responsibilities

• Support clinical trial data review, data cleaning, and query management activities.
• Perform vendor data reconciliation and Local Lab data review.
• Coordinate with internal and external stakeholders; conduct UAT for listings, screens, and edit checks.
• Review clinical data listings and resolve data discrepancies.
• Assist with CRF freeze/lock activities and maintain study documentation in Veeva Vault/eTMF.

Skills

Clinical Data Review

Data Cleaning

Query Management

Vendor Data Reconciliation

CRF Freeze and Lock

UAT for Listings/Screens/Edit Checks

Veeva Vault/eTMF

Clinical Data Workbench

Clinical Data Management Processes

ICH-GCP & 21 CFR Part 11

Cross-functional Collaboration

Written & Verbal Communication

Education

Bachelor's degree in Life Sciences/Pharmacy/Biotechnology/Clinical Research

Tools

Medidata RAVE

Oracle Clinical

J-Review

Spotfire

Veeva Vault

eTMF

Microsoft Office Suite

Microsoft Project

PowerPoint

Job description

Job Summary

We are seeking a Clinical Data Analyst with 2+ 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 2+ 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.