Experienced Clinical Database Programmer – Structured Job Description
Company: Medpace
Function: Data Management
Job ID: 12322
Location: Hyderabad, India
Employment Type: Full-time
Role Summary
The Clinical Database Programmer will be responsible for building, validating, and maintaining clinical trial databases in compliance with industry and company standards. This role supports global clinical studies and plays a key part in ensuring high-quality data management for Phase I–IV clinical research projects.
This position is part of Medpace’s expansion in Hyderabad and offers the opportunity to contribute to the setup of a new operational hub while working on international clinical trials.
Key Responsibilities
1. Clinical Database Development
Develop and program clinical trial databases following company and industry standards
Build and maintain electronic case report forms (eCRFs) aligned with CDASH standards
Ensure accurate database setup for clinical studies
2. Validation & Maintenance
Validate clinical databases to ensure accuracy and compliance
Maintain existing databases throughout the study lifecycle
Ensure adherence to quality and regulatory requirements
3. Technical Support & Study Coordination
Act as the primary technical contact for assigned studies within Data Management teams
Provide programming and database support across study phases
Troubleshoot database-related issues and ensure timely resolution
4. Standards & Library Maintenance
Contribute to the development and maintenance of standard CDASH-compliant CRF libraries
Support continuous improvement of database programming standards and processes
Required Qualifications
Bachelor’s or Advanced degree in Life Sciences, Computer Science, or related field
Minimum 5 years of experience in Medidata Rave study build programming
Strong understanding of clinical data management processes
Required Skills & Technical Expertise
Hands-on experience with Medidata Rave Study Builder (certification preferred)
Knowledge of C# programming (custom functions preferred)
Experience with Veeva EDC (preferred)
Strong attention to detail and quality focus
Excellent communication skills (written and verbal)
Ability to work independently and as part of global study teams
Preferred Attributes
Experience in pharmaceutical or healthcare clinical research environments
Familiarity with CDASH standards and clinical data structures
Strong problem-solving and analytical abilities
Ability to manage multiple studies and deadlines
Role Context
Medpace is a global clinical contract research organization (CRO) supporting Phase I–IV clinical development across multiple therapeutic areas, including oncology, cardiology, metabolic diseases, CNS disorders, and infectious diseases.
This role contributes to the establishment of a new Hyderabad-based operational hub, offering candidates the opportunity to be part of a foundational team with global exposure and long-term growth potential.
Work Environment & Benefits
Flexible work environment
Competitive compensation and benefits
Structured career development pathways
Global exposure to clinical trials
Employee wellness and recognition programs
Opportunity to contribute to a newly launched regional office
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