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Cliantha Research, a reputed full-service Clinical Research Organization (CRO) headquartered in Ahmedabad, India, has announced multiple job openings across clinical research, data management, QA, medical writing, programming, and healthcare roles. This is an excellent opportunity for BPharm, MPharm, MSc, PharmD, MD, and Nursing professionals seeking career growth in a globally compliant CRO environment.
With over 15 years of impeccable regulatory inspection history from USFDA, WHO, MHRA, Health Canada, ANVISA, NABL, and other global agencies, Cliantha Research stands for its core philosophy — “Science with Integrity.”
🧪 Open Positions & Departments
1. Clinical Data Analyst
- Experience: 3–5 years (CDM)
- Qualification: B.Pharm / M.Pharm / Pharm.D
2. Senior Clinical Data Analyst
- Experience: 5–6 years (CDM)
- Qualification: B.Pharm / M.Pharm / Pharm.D
3. Business Development Executive
- Experience: 1–3 years
- Qualification: B.Pharm / M.Pharm / M.Sc / MBA (Marketing) / Pharm.D
4. Late Phase Contracts & Proposal Developer
- Experience: 1–3 years
- Qualification: B.Pharm / M.Pharm / M.Sc
5. SAS Programmer
- Experience: 3–6 years
- Qualification: B.Pharm / M.Pharm with SAS Certification
6. Software Management Officer
- Experience: 1–3 years
- Qualification: BCA / MCA / M.Sc / B.Pharm / M.Pharm
7. Research Scientist (MDMV)
- Experience: 2–6 years
- Qualification: B.Pharm / M.Pharm / M.Sc
8. Trainer
- Experience: 2–4 years
- Qualification: B.Pharm / M.Pharm / M.Sc
9. GCC QA
- Experience: 5–8 years
- Qualification: B.Pharm / M.Pharm / M.Sc
10. CT – QA Auditor
- Experience: 8–12 years
- Qualification: B.Pharm / M.Pharm / M.Sc
11. Medical Writer
- Experience: 1–2 years
- Qualification: M.Pharm (Pharmacology) / Pharm.D
12. Medical Monitor
- Experience: Fresher
- Qualification: MD (Pharmacology)
13. Nurse (Vadodara Location)
- Experience: 1–3 years
- Qualification: B.Sc Nursing / GNM
📍 Job Location
- Ahmedabad, Gujarat
- (Nurse position based in Vadodara)
🎯 Key Responsibilities (Role-Specific)
- Clinical data management, validation & reconciliation
- Regulatory-compliant documentation and audits
- Medical writing for clinical and regulatory deliverables
- Statistical programming and data analysis (SAS)
- QA audits, vendor oversight & compliance monitoring
- Scientific training, protocol review & medical monitoring
- Business development, proposals & client engagement
✅ Eligibility & Skills
- Strong knowledge of ICH-GCP, CDISC, regulatory guidelines
- CRO or clinical research experience preferred
- Excellent documentation, analytical & communication skills
- Ability to work in cross-functional, audit-driven environments
💼 Why Join Cliantha Research?
- Globally audited CRO with strong regulatory credibility
- Exposure to international clinical trials
- Career growth across clinical, regulatory & data domains
- Competitive compensation & professional work culture
📧 How to Apply
Interested and eligible candidates should email their updated resume to:
Last Date to Apply: 10 January 2026