
Cliantha Research, a globally recognized full-service Clinical Research Organization (CRO) headquartered in Ahmedabad, is expanding its team. With an impeccable regulatory track record involving the USFDA, MHRA, and Health Canada, Cliantha offers a high-integrity environment for professionals in clinical and laboratory research.
Current Job Vacancies
Cliantha is looking for talent across various specialized domains, from entry-level reporting to senior project management.
Laboratory & Quality Assurance Roles
- Analyst (Bioanalytical/Lab): * 3–6 years experience (B.Pharm/M.Pharm/M.Sc)
- 2–4 years experience (B.Sc/DMLT)
- QA Auditor (Lab): 3–6 years experience (B.Pharm/M.Pharm/M.Sc)
- CSV-QA (Computer System Validation): 2–6 years experience (B.Pharm/M.Pharm/M.Sc/B.E).
- Trainer: 2–5 years experience (B.Pharm/M.Pharm/M.Sc).
Clinical & Data Management Roles
- Clinical Data Associate (CDA-II) & Sr. CDA: 3–8 years experience (PharmD / M.Pharm / M.Sc).
- Project Coordinator (Clinic): 2–6 years experience (B.Pharm/M.Pharm/M.Sc).
- Report Writer: 1–2 years experience (B.Pharm/M.Pharm/M.Sc).
- Process Excellence: 3–6 years experience (B.Pharm/M.Pharm/M.Sc/B.E).
Senior Leadership Positions
- CT – QA Auditor: 10–12 years experience.
- Project Manager (Consumer Research): 12–15 years experience.
How to Apply
The recruitment is split across two specialized HR departments. Please send your resume to the relevant email addresses based on the role:
- For Laboratory, QA, CSV, and Analyst Roles: 📧 vdesai@cliantha.com / srchauhan1@cliantha.com
- For Clinical Trials, CDA, and Senior Management Roles: 📧 mjunnarkar@cliantha.com / dmirchandani@cliantha.com
Job Location: Ahmedabad, Gujarat.
