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Experienced Clinical Database Programmer (Based In Hyderabad)

7+ years
₹13 – ₹18 LPA
10 July 30, 2025
Job Description
Job Type: Full Time Education: BCS/B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Experienced Clinical Database Programmer
Location: Hyderabad, India
Department: Data Management
Job ID: 11157

Job Summary:
Medpace, a global Clinical Research Organization (CRO), is launching its newest office in Hyderabad and is hiring an experienced, full-time Clinical Database Programmer to join its Data Management team. This role offers a unique opportunity to be part of the founding team at the Hyderabad location, contributing directly to global clinical trials and helping shape the future of Medpace’s operations in India.

If you're looking to make an immediate impact, lead technical efforts, and grow into leadership opportunities, this role offers the perfect platform.

Why Join Medpace in Hyderabad?

  • Founding Team Member: Help lay the groundwork for the Hyderabad office's structure and operations

  • Global Collaboration: Work with international teams on high-impact clinical studies

  • Career Advancement: Be in a prime position for rapid professional growth

  • Well-Established Support: Backed by Medpace’s global infrastructure and SOPs

  • Strong Company Culture: Be part of a stable, development-focused work environment

Key Responsibilities:

  • Develop, program, validate, and maintain clinical trial databases according to company and regulatory standards

  • Contribute to the company’s library of CDASH-compliant CRFs

  • Serve as the primary technical contact for data management on assigned clinical studies

  • Ensure programming quality and consistency across all clinical data systems

Qualifications:

  • Bachelor’s or advanced degree in Life Sciences, Computer Science, or a related field

  • Minimum of 7 years of Rave study build experience in the pharma or healthcare industry

  • Experience in custom function programming using C# is preferred

  • Certified Medidata Rave Study Builder is highly desirable

  • Excellent written and verbal communication skills

  • Strong attention to detail and organizational ability

About Medpace:
Medpace is a leading global CRO providing full-service Phase I–IV clinical development services. Headquartered in Cincinnati, Ohio, Medpace employs over 5,000 professionals across 40+ countries, supporting a wide range of therapeutic areas including oncology, CNS, infectious diseases, cardiology, and endocrinology.

Why Join Medpace?

  • Flexible work environment

  • Competitive compensation and benefits package

  • Comprehensive PTO

  • Defined career growth pathways

  • Employee recognition, wellness, and development initiatives

Awards & Recognition:

  • Forbes: America's Most Successful Midsize Companies (2021–2024)

  • Life Science Leader: CRO Leadership Awards for quality, reliability, and expertise

Estimated Salary: ₹13 – ₹18 LPA (based on Hyderabad market standards and senior-level expertise)