Roles & Responsibilities
• Perform EDC programming using Medidata RAVE or Veeva EDC
• Create, deploy, and maintain clinical study databases
• Configure and test edit checks as per approved specifications
• Review Database Specifications (DBS) and Data Validation Specifications (DVS)
• Support database release activities for production environments
• Ensure compliance with SOPs, GCP, ICH guidelines, and sponsor requirements
• Provide technical support to Clinical Data Management (CDM) teams
• Assist data managers with listings, reports, and operational tasks
• Participate in internal and external study team meetings
• Identify project risks and communicate status to stakeholders
• Maintain high standards of quality, documentation, and performance
Qualification
• Degree in Life Sciences, Pharmacy, or related discipline
Experience
• 1–4 years of experience in clinical database design and deployment
• Minimum 1+ year of hands-on EDC programming experience in Pharma, Biotech, or CRO
• Practical experience with Medidata RAVE or Veeva EDC is mandatory
Skills
• Strong knowledge of EDC systems and clinical database programming
• Understanding of drug development and clinical trial processes
• Knowledge of clinical data management best practices
• Familiarity with global clinical trial workflows and productivity targets
• Good analytical, documentation, and problem-solving skills
• Effective communication and team collaboration abilities
About the Organisation
Atorus Research is a specialized clinical analytics organization delivering high-efficiency, technology-driven solutions to simplify complex clinical trial data. The company supports global studies while ensuring strict compliance with GCP, ICH guidelines, and international regulatory standards.
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