MMS Holdings is hiring a Clinical Data Associate in Bangalore, India. This is a full-time, hybrid opportunity within the Data Management function for candidates with a bachelor’s degree in a scientific, medical, clinical, or related discipline and 1–2 years of clinical data management experience.
MMS Clinical Data Associate Job 2026 – Overview
| Job Detail | Information |
|---|---|
| Company | MMS Holdings |
| Job Title | Clinical Data Associate |
| Department | Data Management |
| Job Type | Full Time |
| Work Model | Hybrid |
| Experience | 1–2 Years |
| Location | Bangalore, Karnataka |
| Education | Bachelor’s Degree in Scientific, Medical, Clinical or Related Discipline |
| Industry | Clinical Research / CRO |
| Job Level | Entry Level |
MMS is a data-focused clinical research organization (CRO) providing clinical data management, biometrics, regulatory and related services to pharmaceutical, biotechnology and medical-device organizations. Its official website describes its data management practice as focused on the design, collection, reconciliation and review of clinical research data, including work across multiple EDC platforms.
About the Clinical Data Associate Role
The Clinical Data Associate will support clinical data management activities and work as part of a project team. The role provides exposure to electronic Case Report Forms (eCRFs), Clinical Data Management Plans (DMPs), edit-check specifications, Electronic Data Capture (EDC) systems, User Acceptance Testing (UAT), study tracking and clinical trial data processes.
This position may suit professionals looking to build or strengthen a career in clinical data management, clinical research, pharmaceutical research and CRO operations.
Clinical Data Associate Responsibilities
Selected candidates may be responsible for:
- Working with MS Office applications for clinical project activities.
- Developing knowledge of ICH guidelines and relevant quality and compliance requirements.
- Gaining exposure to eCRFs and CRF Completion Guidelines.
- Understanding Edit Check Specifications and Data Management Plans.
- Supporting study tracking activities and project metric reports.
- Contributing to User Acceptance Testing (UAT) for EDC and integrated clinical systems.
- Executing UAT test plans and test scripts under project guidance.
- Supporting clinical data management project activities.
- Working collaboratively as a member of the project team.
- Developing an understanding of clinical trial data workflows and pharmaceutical development processes.
- Supporting query and discrepancy management activities.
MMS states that its clinical data management teams work with industry-leading EDC platforms and focus on producing clean, reproducible, fit-for-analysis clinical data.
Eligibility Criteria
Candidates applying for the MMS Clinical Data Associate Jobs in Bangalore should meet the following requirements:
Educational Qualification
- Bachelor’s degree in a scientific, medical, clinical or related discipline is required.
- Master’s degree or PhD is preferred.
Relevant academic backgrounds may include:
- B.Pharm
- M.Pharm
- Pharm.D
- B.Sc
- M.Sc
- Life Sciences
- Biotechnology
- Biochemistry
- Microbiology
- Medicine or allied clinical sciences
- Other relevant scientific or healthcare disciplines
The exact acceptance of a particular degree should be confirmed against the employer’s application requirements.
Experience
- 1–2 years of experience in Clinical Data Management.
- Previous experience with clinical trials is preferred.
- Pharmaceutical or CRO industry experience is required according to the supplied job description.
- Experience with query and discrepancy management is required.
Skills
Candidates should demonstrate:
- Clinical Data Management knowledge
- Clinical trial knowledge
- Query management
- Discrepancy management
- EDC system exposure
- UAT testing
- Test plan and test script execution
- eCRF knowledge
- CRF Completion Guidelines
- Edit check specifications
- Data Management Plans
- MS Office
- Attention to detail
- Documentation and communication skills
- Understanding of clinical research processes
Knowledge of Clinical Research Guidelines
The position provides exposure to important clinical research and quality concepts, including ICH guidelines and 21 CFR Part 11.
The supplied job description also mentions ISO 9001 and ISO 7001. Candidates should verify the exact standards referenced in the employer’s final job posting because the source text may contain a typographical error.
Why This Role Can Be Relevant for Clinical Data Management Careers
Clinical data management is an important component of clinical research because clinical trial data must be collected, reviewed, reconciled and prepared for analysis. MMS describes its data management services as covering the design, collection, reconciliation and review of clinical research data.
For professionals with pharmaceutical, life-science or clinical research backgrounds, experience with EDC, eCRF, edit checks, UAT and query management can provide exposure to core clinical data management workflows.
About MMS Holdings
MMS is a global, data-focused CRO headquartered in the United States, with operations across multiple regions. The company says it was founded in 2006 and has more than 1,000 colleagues worldwide. MMS also lists an India office in Rajajinagar, Bangalore.
The company’s clinical data management services include work involving EDC technologies and clinical data processes across a range of therapeutic areas.
How to Apply
