Global clinical research organization Medpace Clinical Research India is currently hiring for the position of Data Coordinator (Core Laboratory) in Hyderabad and Navi Mumbai. This opportunity is ideal for professionals with 1.5–2 years of Clinical Data Management experience, particularly those with expertise in Electronic Data Capture (EDC), e-CRF review, data cleaning, and clinical trial data validation.
Candidates from Life Sciences, Pharmacy, Biotechnology, Nursing, and Healthcare backgrounds looking to advance their careers in clinical research and clinical data management can explore this promising opportunity.
Job Overview
| Details | Information |
|---|---|
| Position | Data Coordinator (Core Laboratory) |
| Company | Medpace Clinical Research India |
| Location | Hyderabad, Telangana & Navi Mumbai, Maharashtra |
| Experience | 1.5–2 Years |
| Salary | ₹10–11 LPA |
| Employment Type | Full-Time |
| Industry | Clinical Research / CRO / Pharmaceutical |
| Qualification | B.Sc Life Sciences, B.Pharm, Biotechnology, Nursing, Healthcare Related Degree |
Key Responsibilities
The selected candidate will support clinical trial data management activities and ensure data integrity across ongoing studies.
Primary Duties
- Review, validate, and maintain clinical study data in Electronic Data Capture (EDC) systems.
- Conduct data cleaning activities through edit checks and data reviews.
- Manage data change requests and data discrepancy resolution.
- Review electronic Case Report Forms (e-CRFs) for completeness and protocol compliance.
- Coordinate with clinical sites, laboratories, stakeholders, and internal teams.
- Support database maintenance and ongoing quality review processes.
- Track and resolve data-related issues within study timelines.
- Maintain clinical trial documentation and records.
- Ensure compliance with SOPs, ICH-GCP guidelines, and regulatory requirements.
Required Skills
Professionals applying for this Clinical Data Management job should possess:
- Electronic Data Capture (EDC) Systems knowledge
- e-CRF Review and Management experience
- Clinical Data Review and Validation
- Data Cleaning and Query Resolution expertise
- Clinical Trial Documentation skills
- Strong communication and coordination abilities
- Attention to detail and data accuracy
- Understanding of Clinical Research Processes
Eligibility Criteria
Educational Qualification
Candidates should hold a Bachelor’s degree in:
- Life Sciences
- Pharmacy
- Biotechnology
- Nursing
- Healthcare Sciences
- Related Clinical Research disciplines
Experience Required
- Minimum 1.5–2 years of Clinical Data Management experience
- Experience in Core Laboratory Operations preferred
- Previous exposure to CROs, Pharmaceutical, Biotechnology, or Healthcare Research organizations
- Hands-on experience with EDC and e-CRF systems
- Medidata Rave experience is beneficial but not mandatory
Preferred Industry Background
Applicants from the following sectors are encouraged to apply:
- Clinical Research Organizations (CROs)
- Pharmaceutical Companies
- Biotechnology Firms
- Healthcare Research Organizations
- Clinical Data Management Service Providers
Salary and Benefits
Medpace offers a competitive compensation package:
- Annual CTC up to ₹10–11 Lakhs
- Opportunity to work on global clinical trials
- Exposure to advanced Clinical Data Management systems
- Career growth within an international CRO
- Collaborative and research-driven work environment
Why Join Medpace?
Medpace is recognized globally for delivering high-quality clinical research services to pharmaceutical, biotechnology, and medical device companies. Working as a Data Coordinator provides valuable exposure to clinical trial operations, data management systems, regulatory compliance, and global research standards.
Professionals seeking Clinical Data Management jobs in India, EDC specialist roles, Core Laboratory careers, or CRO opportunities can significantly enhance their career trajectory through this position.
How to Apply
