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Database Programmer - Core Laboratory (Based In Hyderabad)

Medpace
0-2 years
Not Disclosed
Hyderabad
10 May 19, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title

Database Programmer – Core Laboratory

Company

Medpace

Location

Hyderabad, India

Department

Data Management / Core Laboratory

Job ID

11925


Role Overview

The Database Programmer – Core Laboratory is responsible for developing, programming, validating, and maintaining clinical trial databases used in global clinical research studies. The role supports data management activities by ensuring accurate database design, edit checks, and programming logic aligned with study requirements and company standards.

This position also serves as the primary programming contact for data management teams, ensuring high-quality database deliverables for clinical trials conducted across multiple therapeutic areas.


Key Responsibilities

1. Clinical Database Development

  • Develop and program clinical trial databases

  • Design and maintain electronic Case Report Forms (eCRFs)

  • Ensure databases meet study and protocol requirements


2. Programming & Validation

  • Program and validate clinical databases according to company standards

  • Implement and maintain:

    • Data models

    • Edit checks

    • Validation rules

  • Ensure accuracy, consistency, and quality of programmed systems


3. Data Quality & Standards Compliance

  • Ensure all programming activities follow:

    • Internal standards

    • Study protocols

    • Data management requirements

  • Maintain high-quality output through meticulous attention to detail


4. Cross-Functional Collaboration

  • Act as primary programming contact for Data Management teams

  • Collaborate with:

    • Data managers

    • Data coordinators

    • Statisticians

    • Other programmers

  • Provide technical support for assigned studies


5. Study Support & Maintenance

  • Maintain ongoing updates and enhancements to clinical databases

  • Support multiple concurrent studies and priorities

  • Ensure timely delivery of programming deliverables


6. Documentation & Technical Support

  • Maintain documentation related to:

    • Database programming

    • Edit checks

    • Validation activities

  • Support study-level technical requirements and troubleshooting


Required Qualifications

Education

  • Bachelor’s degree required, preferably in:

    • Mathematics

    • Information Science

    • Computer Science

    • Related technical field


Required Skills & Competencies

Technical Skills

  • Familiarity with programming languages such as:

    • C#

    • SQL

  • Understanding of clinical database structures and eCRF design

  • Experience with data validation and programming logic


Analytical Skills

  • Strong attention to detail

  • Ability to manage multiple priorities simultaneously

  • Strong problem-solving skills


Communication & Collaboration

  • Excellent verbal and written communication skills

  • Ability to work effectively with cross-functional teams

  • Strong teamwork mindset in a global CRO environment


Work Style

  • Highly organized and detail-oriented

  • Ability to work independently and meet deadlines

  • Flexibility to handle multiple studies and changing priorities


Preferred Attributes

  • Experience in clinical research or CRO environment

  • Exposure to clinical trial data management systems

  • Understanding of clinical trial processes and terminology


Company Overview

Medpace is a global, full-service Contract Research Organization (CRO) supporting Phase I–IV clinical trials across multiple therapeutic areas. The company focuses on accelerating the development of safe and effective medical therapies through scientific rigor and disciplined processes.


Work Environment

  • Global clinical research organization

  • Collaborative, data-driven environment

  • Opportunity to contribute to new office setup in Hyderabad

  • Exposure to international clinical trials and sponsors


Role Summary

The Database Programmer – Core Laboratory role focuses on clinical database development, programming, validation, and maintenance for global clinical trials. It requires strong technical skills in SQL/C#, attention to detail, and the ability to collaborate with cross-functional clinical data teams in a regulated CRO environment.