Cliantha Research, a leading global clinical research organization (CRO), has announced multiple job openings for experienced professionals and freshers across QA/QC, Regulatory Affairs, Medical Writing, Clinical Research, Business Development, Biostatistics, and Medical roles. Candidates with B.Pharm, M.Pharm, M.Sc, Pharm.D, MBA, and MBBS qualifications are invited to apply for exciting opportunities at Ahmedabad and Vadodara.
If you are looking for the latest Cliantha Research jobs 2026, clinical research jobs in Ahmedabad, or pharma jobs for B.Pharm and M.Pharm graduates, this recruitment drive offers excellent career opportunities.
Cliantha Research Recruitment 2026 – Overview
| Particular | Details |
|---|---|
| Company | Cliantha Research |
| Industry | Clinical Research Organization (CRO) |
| Job Type | Full-Time |
| Experience | Fresher to 7 Years |
| Qualification | B.Pharm, M.Pharm, M.Sc, Pharm.D, MBA, MBBS, MD Pharmacology |
| Locations | Ahmedabad, Gujarat & Vadodara, Gujarat |
| Last Date | Apply at the earliest |
| Apply Mode |
Latest Job Openings at Cliantha Research
| Role | Experience | Qualification | Location |
|---|---|---|---|
| QA/QC – Bioanalytical Lab | 2–4 Years | B.Pharm / M.Pharm / M.Sc | Ahmedabad |
| Global Compliance Auditor | 5–7 Years in Clinical Research | B.Pharm / M.Pharm / M.Sc | Ahmedabad |
| Proposal Developer | 2–3 Years | B.Pharm / M.Pharm | Ahmedabad |
| Business Development | 2–4 Years | B.Pharm / MBA | Ahmedabad |
| Medical Writer | 2–4 Years in Protocol Writing | M.Pharm (Pharmacology) / Pharm.D | Ahmedabad |
| Regulatory Affairs | 0–1 Year in Clinical Research | B.Pharm | Ahmedabad |
| Medical Monitor | Fresher | MBBS / MD Pharmacology | Ahmedabad |
| Biostatistician | 2–4 Years | M.Sc (Statistics) | Ahmedabad |
| Clinical Physician | 0–2 Years in Clinical Research | MBBS | Vadodara |
Key Responsibilities
Depending on the position, selected candidates may be responsible for:
- Performing QA/QC activities in bioanalytical laboratories.
- Supporting clinical research and regulatory compliance.
- Preparing clinical study protocols and medical documents.
- Developing proposals for clinical research projects.
- Managing business development activities and client relationships.
- Conducting compliance audits according to international standards.
- Monitoring clinical studies and ensuring participant safety.
- Performing statistical analysis for clinical trial data.
- Supporting regulatory submissions and documentation.
Required Qualifications
Candidates should possess one of the following qualifications:
- B.Pharm
- M.Pharm
- M.Sc
- Pharm.D
- MBA
- MBBS
- MD Pharmacology
Relevant experience ranging from Fresher to 7 years is required depending on the position.
Why Join Cliantha Research?
Working at Cliantha Research offers several career advantages:
- Opportunity to work with a globally recognized Clinical Research Organization.
- Exposure to international clinical research projects.
- Career growth in QA, Regulatory Affairs, Medical Writing, and Clinical Operations.
- Professional learning and development opportunities.
- Collaborative work environment.
- Competitive compensation and employee benefits.
How to Apply
Interested and eligible candidates should send their updated resume to:
Email: jobs@cliantha.com
