Apply for Clinical Data Manager job at Emmes Group Bengaluru with CRO experience, EDC systems knowledge, and clinical research expertise.
Clinical Data Manager Recruitment 2026
Emmes Group is inviting applications for the position of Clinical Data Manager in Bengaluru, India. Candidates with experience in clinical data management, EDC systems, CDISC standards, and CRO/pharmaceutical environments are encouraged to apply.
Emmes Group is a globally recognized clinical research organization with more than 47 years of scientific excellence in cell and gene therapy, vaccines, infectious diseases, rare diseases, neuroscience, and ophthalmology.
Job Details
| Particulars | Details |
|---|---|
| Job Title | Clinical Data Manager |
| Company Name | Emmes Group |
| Job Location | Bengaluru, Karnataka, India |
| Department | Clinical Operations |
| Employment Type | Regular Full-Time |
| Job ID | 2975 |
| Industry | Clinical Research / CRO |
| Experience Required | 3+ Years |
| Qualification | Bachelor’s / Master’s Degree |
| Eligible Streams | Life Sciences, Health Information Management, Computer Science |
| Work Mode | Full-Time |
| Salary | As Per Company Standards |
About Emmes Group
Emmes Group combines science, technology, and innovation to accelerate clinical research and global healthcare solutions. Through its business units Emmes CRO and Veridix AI, the company modernizes clinical trials using advanced analytical and data-driven technologies.
The organization works in multiple therapeutic areas including vaccines, neuroscience, rare diseases, ophthalmology, infectious diseases, and gene therapy.
Key Responsibilities
- Develop and maintain Data Management Plans (DMPs) and validation specifications.
- Design and review CRFs/eCRFs with clinical teams and vendors.
- Manage Electronic Data Capture (EDC) systems like Medidata Rave, Oracle InForm, Veeva, and REDCap.
- Perform data cleaning, query management, and issue resolution activities.
- Ensure timely database lock and accurate data delivery.
- Coordinate with CROs, vendors, and laboratories for compliant data operations.
- Collaborate with clinical, regulatory, safety, and biostatistics teams.
- Ensure compliance with FDA 21 CFR Part 11 and ICH GCP guidelines.
- Support audits, inspections, and internal quality reviews.
- Maintain study documentation for regulatory inspection readiness.
Required Skills
- Strong experience with EDC platforms such as Medidata Rave, Veeva, and Oracle InForm.
- Knowledge of CDISC standards including SDTM and ADaM.
- Familiarity with MedDRA and WHODrug coding standards.
- Experience in database lock, edit checks, and query management.
- Knowledge of SAS, SQL, or related data handling tools is an added advantage.
- Excellent organizational and communication skills.
- Strong problem-solving and team collaboration abilities.
Educational Qualification
Required Qualification
- Bachelor’s Degree in:
- Life Sciences
- Health Information Management
- Computer Science
- Related Field
Preferred Qualification
- Master’s Degree in relevant discipline
Experience Required
| Experience | Requirement |
|---|---|
| Clinical Data Management | Minimum 3 Years |
| CRO / Pharma / Biotech Experience | Preferred |
| EDC Systems & CDISC Standards | Preferred |
Why Join Emmes Group?
- Opportunity to work with a globally recognized CRO
- Exposure to advanced clinical technologies and AI platforms
- Career growth in international clinical research projects
- Collaborative and innovation-driven work culture
- Contribute to life-changing healthcare solutions
How to Apply
Interested candidates can apply online through the official career portal of Emmes Group.
