Emmes Group is hiring a Clinical Data Manager (CDM) for its Clinical Operations team in Bengaluru, India. The role is focused on managing clinical trial data, including data collection, validation, cleaning, query management, database lock and compliant data delivery.
Candidates with a Bachelor’s degree in Life Sciences, Health Information Management, Computer Science or a related field and 4–6 years of clinical data management experience can apply.
Clinical Data Manager Job Overview
| Particulars | Details |
|---|---|
| Company | Emmes Group |
| Job Role | Clinical Data Manager |
| Department | Clinical Operations |
| Job Location | Bengaluru, India |
| Experience | 4–6 Years |
| Qualification | Bachelor’s Degree; Master’s preferred |
| Employment Type | Regular, Full-Time |
| Job ID | 3598 |
| Industry | Clinical Research / CRO / Life Sciences |
About the Clinical Data Manager Role
The Clinical Data Manager will oversee the collection, processing, cleaning and management of clinical trial data.
The position is responsible for ensuring that clinical data is accurate, complete and verifiable according to study protocols, regulatory requirements and Good Clinical Practice (GCP) guidelines.
The role involves collaboration with clinical, regulatory, biostatistics, safety teams, CROs, EDC vendors and central laboratories.
Key Responsibilities
Clinical Data Management
- Develop and maintain Data Management Plans (DMPs).
- Prepare data validation specifications and other study-related documentation.
- Design and review CRFs/eCRFs with clinical teams and vendors.
- Perform and review data cleaning activities.
- Generate and resolve clinical data queries.
- Support issue resolution and data quality activities.
- Ensure timely database lock and delivery of clinical data.
EDC Systems
The Clinical Data Manager will support the setup, validation and maintenance of electronic data capture systems, including:
- Medidata Rave
- Oracle InForm
- Veeva
- REDCap
Experience with EDC systems is an important requirement for this position.
Cross-Functional Collaboration
- Coordinate with CROs, EDC vendors and central laboratories.
- Work with clinical, regulatory, biostatistics and pharmacovigilance/safety teams.
- Participate in study team meetings.
- Contribute to project timelines and risk management.
- Ensure data deliverables remain aligned with study requirements.
Compliance & Quality
- Ensure compliance with applicable regulatory requirements.
- Follow FDA 21 CFR Part 11 and ICH-GCP requirements.
- Participate in audits and data review meetings.
- Support internal quality checks.
- Maintain complete documentation for inspection readiness.
Educational Qualification
Required
Bachelor’s degree in any of the following or a related discipline:
- Life Sciences
- Health Information Management
- Computer Science
- Related field
Preferred
- Master’s degree in Life Sciences
- Master’s degree in Health Information Management
- Master’s degree in Computer Science
- Related discipline
Experience Required
Candidates should have approximately 4–6 years of experience in Clinical Data Management.
Experience in the following industries is preferred:
- Pharmaceutical
- Contract Research Organization (CRO)
- Biotechnology
Prior experience with EDC systems and CDISC standards is also preferred.
Required Skills
Candidates should have knowledge or experience in:
- Clinical Data Management
- EDC systems
- Medidata Rave
- Veeva
- Oracle InForm
- CDISC standards
- SDTM
- ADaM
- Data cleaning
- Query management
- Edit checks
- Database lock
- Clinical trial data review
- Regulatory compliance
- ICH-GCP
- FDA 21 CFR Part 11
Familiarity with MedDRA and WHODrug is also expected.
Knowledge of SAS, SQL or other data-handling languages will be an additional advantage.
Key Skills
- Strong attention to detail
- Excellent organizational skills
- Good communication and interpersonal skills
- Ability to manage multiple projects
- Ability to work with deadlines
- Proactive problem-solving approach
- Team-oriented mindset
- Strong clinical data management knowledge
Job Location
Bengaluru, Karnataka, India
The position is listed under Clinical Operations and is a Regular Full-Time opportunity.
How to Apply for Emmes Group Clinical Data Manager Job 2026?
Interested and eligible candidates can apply for the Clinical Data Manager position through the official Emmes Group careers channel.
Candidates should ensure that their resume highlights relevant experience in clinical data management, EDC systems, database lock, query management, CDISC and clinical trial data operations.
About Emmes Group
Emmes Group is a clinical research organization and healthcare technology company working across areas including cell and gene therapy, vaccines, infectious diseases, ophthalmology, rare diseases and neuroscience.
The organization operates through its business units Emmes, a full-service CRO, and Veridix AI, which focuses on technology, data and analytical solutions for clinical research.
Important Note
The job information provided lists 4–6 years of clinical data management experience as the required experience range. Candidates should review the official job posting for the latest eligibility criteria and application details before applying.