Quanticate is recruiting for the position of Clinical Data Coordinator 2 in Bengaluru, Karnataka. The opportunity is suitable for professionals with 2–6 years of experience in Clinical Data Management (CDM), particularly those with hands-on experience using clinical data management systems such as Medidata Rave, Oracle Clinical or Inform.
The selected candidate will support end-to-end clinical data management activities across multiple studies, including database testing, CRF review, data query resolution, quality control and study close-out activities.
Quanticate Recruitment 2026 – Job Details
| Particulars | Details |
|---|---|
| Company | Quanticate |
| Job Title | Clinical Data Coordinator 2 |
| Job Category | Clinical Data Management |
| Industry | Clinical Research / Contract Research |
| Department | Research & Development |
| Qualification | Not listed in the supplied job description |
| Experience | 2–6 Years |
| Salary | ₹6–15 LPA |
| Job Location | Bengaluru (Koramangala) |
| Work Mode | Hybrid |
| Employment Type | Full-Time, Permanent |
| Number of Openings | 3 |
Position: Clinical Data Coordinator 2
Quanticate is looking for experienced Clinical Data Management professionals to support clinical studies and maintain data quality, accuracy and regulatory compliance.
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Key Responsibilities
- Support end-to-end Clinical Data Management activities across multiple studies.
- Assist with database testing and validation before study activation.
- Prepare and maintain study-specific Data Management documentation.
- Review Case Report Forms (CRFs) to identify data inconsistencies, errors and missing information.
- Raise, track and resolve data queries and Data Clarification Forms (DCFs).
- Manage self-evident queries and allowable data changes within the database.
- Perform quality control checks on data entry and database outputs.
- Support study close-out activities, including archival documentation.
- Ensure compliance with SOPs, ICH-GCP guidelines, regulatory requirements and client standards.
- Contribute to process improvement initiatives and data management best practices.
- Perform medical coding activities when assigned.
- Collaborate with offshore data processing and programming teams.
- Provide project updates and track progress using reports and metrics.
- Handle additional tasks supporting project and team objectives.
Eligibility Criteria
Candidates should have:
- 2–6 years of experience in Clinical Data Management or a similar role.
- Strong understanding of Clinical Data Management processes.
- Knowledge of ICH-GCP guidelines and regulatory requirements related to data handling.
- Hands-on experience with at least one Clinical Data Management system, such as:
- Oracle Clinical
- Medidata Rave
- Inform
- Experience supporting multiple studies or managing competing priorities is preferred.
Required Skills
- Clinical Data Management (CDM).
- Clinical trial data management.
- Electronic Data Capture (EDC).
- Medidata Rave.
- Clinical database testing and validation.
- CRF review and data query management.
- Data quality control.
- Medical coding.
- ICH-GCP and regulatory compliance.
- Microsoft Word and Excel.
- Analytical thinking and attention to detail.
- Written and verbal communication.
- Organizational and time-management skills.
- Ability to collaborate with offshore and remote teams.
