Medpace is hiring for four positions in its Data Management and Biometrics teams in Navi Mumbai, Maharashtra. The openings include Clinical Database Programmer, Clinical Data Coder, Clinical Data Review Associate, and Clinical Database Designer.
These opportunities are intended for candidates with relevant backgrounds in life sciences, computer science, nursing, or pharmacy, depending on the position. The roles involve clinical trial database programming, medical coding, clinical data review, and electronic clinical database design.
Medpace Recruitment 2026: Job Details
| Job Detail | Information |
|---|---|
| Company | Medpace |
| Job Location | Navi Mumbai, Maharashtra, India |
| Department | Data Management |
| Total Positions | 4 |
| Industry | Clinical Research / CRO |
| Work Environment | Office-based |
| Company Headquarters | Cincinnati, Ohio, USA |
Positions Available at Medpace
1. Clinical Database Programmer
Job ID: 12324
The Clinical Database Programmer will develop, program, validate, and maintain clinical trial databases in accordance with company standards.
Responsibilities:
- Develop, program, validate, and maintain clinical trial databases.
- Maintain and contribute to the company’s library of CDASH-compliant Case Report Forms (CRFs).
- Provide technical support to Data Management teams for assigned studies.
- Ensure programming quality and compliance with company standards.
Eligibility and Qualifications:
- Bachelor’s or advanced degree in Life Sciences, Computer Science, or an equivalent qualification.
- Rave study build or Veeva EDC experience in the pharmaceutical or healthcare sector is preferred.
- Custom function programming experience using C# is preferred.
- Medidata Rave Study Builder certification is preferred.
- Excellent verbal and written communication skills.
- Strong attention to detail.
2. Clinical Data Coder
Job ID: 12327
The Clinical Data Coder will code and review medical terms and medications using industry-standard and company-specific dictionaries.
Responsibilities:
- Perform accurate coding and review of medical terms and medications.
- Coordinate dictionary selection and develop coding guidelines.
- Ensure consistent coding practices across clinical studies.
- Collaborate with Data Management teams and Medical Monitors to resolve coding queries.
- Generate coding reports, monitor timelines, and ensure quality and timely delivery of study deliverables.
Eligibility and Qualifications:
- Bachelor’s degree in Nursing or Pharmacy, or an advanced clinical degree.
- At least 2 years of clinical nursing or pharmacy experience involving direct patient care in relevant therapeutic areas.
- Relevant therapeutic experience may include Hematology/Oncology, Metabolic, Infectious Disease, Nephrology, Neurology/Musculoskeletal, or Cardiovascular care.
- ICU experience is preferred.
- Hands-on Hematology/Oncology experience, including administration and management of treatment-related side effects, is required.
- Hospital or clinical research coding experience and familiarity with MedDRA and WHO Drug dictionaries are additional advantages.
3. Clinical Data Review Associate – Entry (Nurses Wanted)
Job ID: 12326
This entry-level opportunity is designed for nursing graduates seeking to apply their clinical knowledge and healthcare experience to clinical trial data review.
Responsibilities:
- Review clinical data collected during clinical trials.
- Generate and resolve queries to clarify inconsistent clinical data.
- Coordinate with Data Management teams to support query resolution.
- Contribute to the development of clinical review guidelines.
- Develop specialization in therapeutic areas such as Oncology, Infectious Disease, Cardiology, Endocrine, and Hematology.
Eligibility and Qualifications:
- Bachelor’s degree in Nursing.
- Broad knowledge of medical terminology.
- Experience working with or reviewing clinical data.
- Clinical experience in a hospital or healthcare setting.
- General knowledge of the pharmaceutical industry and regulations concerning electronic records.
Medpace provides training and support to help candidates transition into this role.
4. Clinical Database Designer
Job ID: 12325
The Clinical Database Designer will develop and maintain electronic Case Report Form (eCRF) specifications, edit check specifications, and clinical database design documentation throughout the study lifecycle.
Responsibilities:
- Maintain standard eCRF and Edit Check Specification templates in accordance with CDISC standards.
- Develop and maintain study-specific eCRF specifications from database build through database lock.
- Develop and maintain edit check specifications, including change requests.
- Validate eCRFs and edit checks against specifications and document testing scenarios.
- Coordinate with Data Managers, sponsors, and Clinical Database Programmers.
- Develop project-level reports using EDC reporting tools such as Business Objects and JReview.
- Lead internal and external eCRF specification review meetings.
- Explain technical design decisions and discuss database design options with sponsors.
Eligibility and Qualifications:
- Bachelor’s or advanced degree in Life Sciences, Computer Science, or an equivalent qualification.
- At least 1 year of experience building specifications and/or performing User Acceptance Testing (UAT) for EDC databases.
- Excellent verbal and written communication skills.
- Strong attention to detail.
Required Skills Across the Openings
The required skills depend on the position:
- Clinical Database Programmer: Clinical database programming, clinical trial database validation, CDASH, Medidata Rave or Veeva EDC; C# experience is preferred.
- Clinical Data Coder: Medical terminology coding, medication coding, clinical dictionary knowledge, and therapeutic-area experience.
- Clinical Data Review Associate: Clinical data review, medical terminology, clinical query resolution, and nursing experience.
- Clinical Database Designer: eCRF specifications, edit checks, CDISC standards, EDC database testing, and stakeholder coordination.
