Medpace, a global Contract Research Organization (CRO), is hiring for multiple positions across its Navi Mumbai and Hyderabad offices in India. The current openings span Clinical Data Management, Biostatistics, Clinical Trial Management, Imaging Services, Clinical Operations, and Clinical Database Programming.
Medpace is seeking candidates from Life Sciences, Pharmacy, Nursing, Computer Science, Statistics, Biomedical Engineering, and related backgrounds for entry-level and experienced positions.
Candidates interested in clinical research, clinical data management, SAS programming, clinical database development, and clinical operations can explore the following opportunities.
Medpace Recruitment 2026 – Job Details
| Particulars | Details |
|---|---|
| Company | Medpace |
| Industry | Clinical Research / CRO |
| Job Location | Navi Mumbai & Hyderabad, India |
| Job Type | Full-Time |
| Work Mode | Office-Based |
| Departments | Data Management, Biostatistics, Clinical Operations, Clinical Trial Management, Imaging Services |
| Experience | Freshers to Experienced Professionals, depending on the position |
| Official Website | https://www.medpace.com/ |
Medpace Job Openings 2026 – Multiple Positions
Navi Mumbai Job Openings
| Position | Job ID | Experience / Eligibility |
|---|---|---|
| Clinical Database Designer | 12325 | Minimum 1 year EDC specifications or UAT experience |
| Clinical Data Review Associate | 12326 | Bachelor’s Degree in Nursing |
| Clinical Data Coder | 12327 | 2+ years of clinical nursing or pharmacy experience |
| Experienced SAS Programmer | 12319 | 5+ years of SAS experience |
| Clinical Database Programmer | 12324 | Life Sciences or Computer Science background |
| SAS Programmer | 12315 | SAS knowledge; 1–2 years preferred |
| Data Coordinator – Core Laboratory | 11924 | 1–2 years preferred |
| Project Coordinator – Core Laboratory | 11928 | Biomedical Engineering background |
| Clinical Trial Manager | 11922 | At least 2 years of clinical trial management experience |
| Site Payments Processor | 12313 | At least 1 year of relevant finance or accounting experience |
| Data Coordinator – Core Laboratory | 11923 | Life Sciences, Pharmacy or healthcare background |
| Database Programmer – Core Laboratory | 11926 | Bachelor’s degree; C# and SQL preferred |
Hyderabad Job Openings
| Position | Job ID | Experience / Eligibility |
|---|---|---|
| Experienced Clinical Database Programmer | 12322 | Minimum 6 years of Medidata Rave study build experience |
| Project Coordinator – Core Laboratory | 11936 | Biomedical Engineering background |
| Database Programmer – Core Laboratory | 11925 | Bachelor’s degree; C# and SQL preferred |
| Data Coordinator – Core Laboratory | 11923 | Life Sciences, Pharmacy or healthcare background |
| Associate Clinical Trial Manager – PhD / Post-Doc | 11837 | PhD in Life Sciences with relevant research experience |
Job Responsibilities
Responsibilities vary by position and department.
1. Clinical Data Management
- Develop and maintain electronic Case Report Forms (eCRFs) and edit check specifications.
- Review clinical trial data and resolve data discrepancies.
- Perform clinical database validation and testing.
- Maintain clinical data management documents and data transfers.
- Perform medical terminology and medication coding using standard dictionaries.
2. Clinical Database Programming
- Develop, program, validate and maintain clinical trial databases.
- Maintain CDASH-compliant CRF libraries.
- Develop data models and electronic CRFs.
- Provide technical support to Data Management teams.
- Work with Medidata Rave, Veeva EDC, C# and SQL, depending on the role.
3. Biostatistics and SAS Programming
- Develop SAS programs for analysis datasets, tables, listings and figures.
- Validate and maintain mapped databases.
- Program edit checks for external data.
- Support external data integration and database specifications.
4. Clinical Trial Management and Project Coordination
- Coordinate global study activities and project timelines.
- Maintain study status reports and project documentation.
- Communicate with sponsors, study sites and internal teams.
- Manage project deliverables, study vendors and site quality.
- Coordinate project meetings and maintain meeting minutes.
5. Clinical Operations and Site Payments
- Process and reconcile clinical trial site payments.
- Maintain site payment records and reporting.
- Coordinate site-specific agreements and amendments.
- Track and reconcile invoices.
Eligibility and Qualifications
Medpace has openings for candidates with the following educational backgrounds:
- B.Pharm / Pharmacy
- Nursing
- Life Sciences
- Biomedical Engineering
- Computer Science
- Mathematics and Statistics
- Health Informatics
- Data Science
- Relevant advanced degrees, including PhD and Postdoctoral research qualifications.
Position-Wise Experience Requirements
| Position | Key Eligibility |
|---|---|
| Clinical Database Designer | At least 1 year of EDC specification development and/or UAT experience |
| Clinical Data Review Associate | Bachelor’s in Nursing; hospital or healthcare clinical experience |
| Clinical Data Coder | Bachelor’s in Nursing or Pharmacy; 2+ years of relevant clinical experience |
| Experienced SAS Programmer | 5+ years of SAS experience; CDISC knowledge |
| SAS Programmer | SAS knowledge; 1–2 years preferred |
| Experienced Clinical Database Programmer | 6+ years of Medidata Rave study build experience |
| Clinical Trial Manager | 2+ years of clinical trial management experience |
| Data Coordinator | 1–2 years in pharmaceutical or CRO settings preferred |
| Site Payments Processor | 1+ year in finance, accounting, treasury or business-related fields |
| Associate Clinical Trial Manager | PhD in Life Sciences with relevant therapeutic-area research experience |
Required Technical Skills
Depending on the position, candidates may benefit from the following skills and domain knowledge:
- Clinical Data Management
- Electronic Data Capture (EDC)
- Medidata Rave
- Veeva EDC
- CDISC and CDASH Standards
- SAS Programming
- C# Programming
- SQL
- MedDRA and WHO Drug Dictionaries
- Clinical Trial Data Review
- Clinical Database Validation
- Microsoft Excel and Word
- Clinical Trial Management
- ICH-GCP and electronic records regulations
BELOW ROLES ARE FOR FRESHERS
1. Clinical Data Review Associate (Job ID: 12326) – Entry-level position for B.Sc Nursing / Bachelor’s in Nursing graduates. Training and support are provided.
2. Clinical Database Programmer (Job ID: 12324) – No minimum experience specified; Life Sciences or Computer Science graduates may be eligible, preferably with relevant EDC knowledge.
3. Project Coordinator – Core Laboratory (Job IDs: 11928 / 11936) – Prior research experience is preferred, not mandatory. Biomedical Engineering graduates can apply.
4. Database Programmer – Core Laboratory (Job ID: 11925) – No minimum experience specified; Bachelor’s degree required, preferably in Mathematics or Information Science.
5. Database Programmer – Core Laboratory (Job ID: 11926) – No minimum experience specified; Bachelor’s degree required, preferably in Mathematics or Information Science.
