Cliantha Research is hiring talented professionals across multiple roles in Ahmedabad. This is an excellent opportunity for candidates from pharmacy, life sciences, and medical backgrounds to join a globally recognized clinical research organization (CRO).
Whether you’re a fresher or an experienced professional in GCP auditing, biometrics, pharmacovigilance, or business development, Cliantha offers a dynamic work environment with exposure to global clinical trials and compliance standards.
Open Positions at Cliantha Research
- QA Auditor – Lab (2–4 years)
- Trainer (2–4 years)
- Global Compliance Cell Auditor – GCP (8–10 years)
- Report Writer – Biometrics (0–2 years)
- Medical Monitor (Freshers – MBBS + MD Pharmacology)
- Business Development – Consumer Research (2–3 years)
- Proposal Developer – Late Phase (2–3 years)
📍 Location: Ahmedabad, Gujarat
Key Responsibilities
Quality Assurance & GCP Roles
- Conduct internal and external audits as per GCP and regulatory guidelines
- Handle deviations, CAPA, and compliance documentation
- Ensure adherence to global standards like ICH-GCP, USFDA, EMA
Trainer
- Deliver training sessions on clinical processes and compliance
- Develop training modules and SOP-based learning content
Biometrics Report Writer
- Prepare clinical study reports, tables, listings, and figures (TLFs)
- Support statistical teams with documentation and data interpretation
Medical Monitor
- Oversee clinical trial safety and protocol compliance
- Provide medical insights and support for study conduct
Business Development / Proposal Developer
- Identify new business opportunities in clinical research
- Prepare proposals for late-phase clinical trials
- Coordinate with internal stakeholders for project execution
Qualifications Required
- B.Pharm / M.Pharm / Pharm.D / M.Sc (Life Sciences)
- MBBS + MD Pharmacology (for Medical Monitor role)
- Strong knowledge of clinical trials, GCP, regulatory compliance
- Experience in auditing, biometrics, or business development (role-specific)
- Excellent communication and documentation skills
Benefits of Working at Cliantha Research
- Opportunity to work in a global CRO environment
- Exposure to international clinical trials and regulatory frameworks
- Career growth in clinical research, pharmacovigilance, and biometrics
- Competitive salary packages and learning opportunities
- Collaborative and innovation-driven workplace
Salary Insight (INR)
- Freshers: ₹3 – ₹6 LPA
- Mid-Level (2–4 yrs): ₹5 – ₹9 LPA
- Senior Roles (8–10 yrs): ₹12 – ₹20 LPA
(Salary may vary based on role and experience)
How to Apply
Interested candidates can share their updated CV to:
📧 vdesai@cliantha.com
📧 mjunnarkar@cliantha.com
