Cliantha Research has announced a walk-in interview for the position of Clinical Data Analyst at its Ahmedabad facility in Gujarat. The opportunity is suitable for candidates with experience in clinical data management, clinical database activities and clinical research operations.
The role involves preparing study-specific documentation, designing and reviewing Case Report Forms (CRFs), performing User Acceptance Testing (UAT), resolving clinical data discrepancies and coordinating with study teams to maintain data quality.
Candidates with 1 to 6 years of experience and qualifications such as B.Pharm, M.Sc or M.Pharm can consider this opportunity. According to the recruitment listing, the advertised salary range is ₹3.5 lakh to ₹8.5 lakh per annum.
Cliantha Research Recruitment 2026 – Job Highlights
| Particular | Details |
|---|---|
| Company | Cliantha Research |
| Job Position | Clinical Data Analyst |
| Department | Clinical Data Management (CDM) |
| Job Location | Ahmedabad, Gujarat |
| Experience | 1–6 Years |
| Qualification | B.Pharm / M.Sc / M.Pharm |
| Employment Type | Full Time, Permanent |
| Salary Range | ₹3.5–8.5 LPA, as advertised |
| Vacancies | 5 |
| Recruitment Type | Walk-In Interview |
| Interview Date | 10 October 2026 |
| Interview Time | 9:30 AM–3:00 PM |
| Contact Person | Mukund Junnarkar |
About Cliantha Research
Cliantha Research operates in the clinical research and contract research sector. This recruitment is for its Clinical Data Management function, which supports clinical studies through database management, data validation, discrepancy resolution, quality checks and study documentation.
Job Description: Clinical Data Analyst
The Clinical Data Analyst will coordinate with the assigned Study Lead and contribute to the progress of clinical data management activities. The role covers both paper-based and Electronic Data Capture (EDC) studies.
The selected candidate will help ensure that clinical study data is accurate, consistent, properly documented and managed according to applicable procedures and project requirements.
Key Responsibilities
1. Clinical Data Management Documentation
- Prepare, maintain and update study-specific documents.
- Develop or maintain Data Management Plans and Data Validation Plans.
- Support database design specifications and external data handling plans.
- Maintain project documentation according to applicable procedures.
- Ensure appropriate archiving of study data and documents.
2. CRF Design and Database Testing
- Design and review Case Report Forms for paper-based and EDC studies.
- Track the receipt of subject CRFs for paper-based studies.
- Perform User Acceptance Testing (UAT) of study databases.
- Check that electronic data entry screens are consistent with the relevant CRFs.
- Identify discrepancies between study requirements and database functionality.
3. Clinical Data Review and Query Management
- Identify and resolve data discrepancies through manual and computerised checks.
- Generate data queries and review responses.
- Update and verify Data Clarification Forms (DCFs) and external DCFs for paper-based studies.
- Perform quality control checks on assigned clinical studies.
- Coordinate with study team members to resolve data-related issues.
4. External Data and Safety Reconciliation
- Manage external clinical data and perform applicable reconciliation activities.
- Resolve queries associated with external data.
- Perform Serious Adverse Event (SAE) reconciliation.
- Follow up on discrepancies related to SAE information.
- Perform medical coding of terms reported on Case Report Forms.
5. EDC Training and Study Coordination
- Train clinical sites on the use of study-specific EDC databases.
- Process requests for role-specific database access.
- Coordinate with programmers, statisticians, monitors, Clinical Research Associates (CRAs) and external teams.
- Follow assigned training schedules.
- Maintain awareness of relevant Data Management SOPs and work procedures.
Educational Qualification
The recruitment listing specifies the following educational backgrounds:
- B.Pharm in any specialization.
- M.Sc in a science specialization.
- M.Pharm in any specialization.
Candidates should review the employer’s requirements to confirm that their qualification is suitable for the position.
Experience Requirements
The advertised experience range is 1 to 6 years.
Relevant experience may include clinical data management, clinical database activities, CRF design, EDC systems, data validation, query management and clinical study documentation.
Required Skills
Candidates should have knowledge or experience in the following areas:
- Clinical Data Management (CDM)
- Case Report Forms (CRFs)
- Electronic Data Capture (EDC)
- User Acceptance Testing (UAT)
- Data Validation Plans
- Database design specifications
- Clinical data discrepancy management
- Data quality control
- External data reconciliation
- Serious Adverse Event reconciliation
- Medical coding
- SOP compliance and documentation
- Clinical research team coordination
- Data archiving
Work Location
The position is based at Cliantha Research in Ahmedabad, Gujarat.
Interview venue:
Cliantha Research, La Costa, TP 86, FP 21 & 47, Off S.P. Ring Road, Near Lakshya International School, Sarkhej, Ahmedabad – 382210, Gujarat, India.
Salary / CTC
The recruitment listing advertises a salary range of ₹3.5 LPA to ₹8.5 LPA. The actual compensation may depend on the candidate’s relevant experience, skills and the employer’s offer.
Walk-In Interview Details
| Particular | Details |
|---|---|
| Company | Cliantha Research |
| Position | Clinical Data Analyst |
| Date | 10 October 2026 |
| Time | 9:30 AM–3:00 PM |
| Venue | Cliantha Research, La Costa, Sarkhej, Ahmedabad – 382210 |
| Contact Person | Mukund Junnarkar |
| Number of Openings | 5 |
Documents to Carry
The supplied recruitment listing does not provide a specific document checklist. Candidates should carry an updated resume and relevant educational and experience documents, and confirm any additional requirements with the recruiter before attending.
How to Apply for Cliantha Research Recruitment 2026
Interested candidates can attend the walk-in interview at the Ahmedabad venue on 10 October 2026 between 9:30 AM and 3:00 PM.
Candidates should ensure that their qualifications and experience match the requirements of the Clinical Data Analyst role before attending.
The vacancy was advertised on Naukri. Candidates can review the employer’s recruitment listings here:
Important Details Before Applying
- The position is Clinical Data Analyst.
- The advertised experience range is 1–6 years.
- The advertised salary is ₹3.5–8.5 LPA.
- Five openings are listed.
- The role involves CRFs, EDC, UAT, data queries and clinical data quality.
- The interview is scheduled for 10 October 2026.
- The venue is in Sarkhej, Ahmedabad.
- Confirm the interview schedule and any additional requirements before travelling.
Frequently Asked Questions
1. What position is Cliantha Research hiring for?
Cliantha Research is recruiting for the position of Clinical Data Analyst.
2. Where is the job located?
The position is based in Ahmedabad, Gujarat.
3. What is the required experience?
The recruitment listing specifies 1–6 years of experience.
4. What qualifications are accepted?
The listing mentions B.Pharm, M.Sc and M.Pharm qualifications.
5. What is the advertised salary?
The advertised salary range is ₹3.5–8.5 LPA.
6. When is the walk-in interview?
The interview is scheduled for 10 October 2026.
7. What are the interview timings?
The listed timings are 9:30 AM to 3:00 PM.
8. What does the Clinical Data Analyst do?
The role involves clinical study documentation, CRF design, database testing, data validation, query management, reconciliation and data quality control.
9. What is EDC?
EDC stands for Electronic Data Capture, a system used to collect and manage clinical study data electronically.
10. How many vacancies are listed?
The recruitment listing mentions five openings.
Important Note
This article is based on the supplied recruitment listing. Salary, vacancy numbers, eligibility criteria and interview arrangements may change. Candidates should confirm the latest details with Cliantha Research before attending the walk-in interview.