Clinical Data Manager (CDM)

Roles & Responsibilities
• Manage end-to-end Clinical Data Management (CDM) activities for global clinical trials
• Perform User Acceptance Testing (UAT) for EDC systems (Medidata RAVE)
• Oversee study conduct and ongoing data review cycles
• Handle query management and discrepancy resolution
• Conduct data validation and review edit checks
• Support database freeze, lock, and close-out activities
• Coordinate with Clinical Research Associates (CRAs), Project Managers (PMs), and sponsor teams
• Ensure compliance with ICH-GCP guidelines and data integrity standards
• Assist in study close-out and archival procedures
• Maintain accurate documentation across the clinical database lifecycle

Qualification
• B.Pharm (Bachelor of Pharmacy) / M.Pharm (Master of Pharmacy) / Life Sciences / Clinical Research or equivalent (preferred)

Experience
• Minimum 3+ years of experience in Clinical Data Management
• Hands-on experience with Medidata RAVE EDC
• Experience in UAT testing and database validation
• Exposure to study conduct phase and database lock activities
• Experience coordinating with sponsors and cross-functional teams

Skills
• Strong query management and discrepancy handling expertise
• Knowledge of data validation checks and edit check review
• Understanding of clinical trial lifecycle and CDM processes
• Familiarity with database freeze and lock procedures
• Strong analytical and problem-solving skills
• Effective stakeholder communication and coordination

Walk-In Interview Details
Date: 23rd February
Time: 10:30 AM – 2:00 PM
Venue: Jubilee Hills Check Post Rd, Jawahar Colony, Jubilee Hills, Hyderabad, Telangana 500033

About the Organization
OrciMed is a clinical research organization delivering data management and clinical operations services for global trials. The company focuses on regulatory compliance, data integrity, and efficient clinical database lifecycle management to support international pharmaceutical and biotech sponsors.