Cliantha Research is a leading global Contract Research Organization (CRO) specializing in Bioavailability (BA), Bioequivalence (BE), and clinical research services. With a strong reputation (⭐ 4.0+ ratings), Cliantha offers end-to-end clinical trial solutions, regulatory compliance, and cutting-edge research in pharmaceuticals.
📍 Location: Ahmedabad, India
🌐 Industry: Clinical Research / Contract Research
Job Openings at Cliantha Research
1. Global Project Manager (BA/BE Studies)
Experience: 1-2 years | Salary: ₹2-3.5 LPA
Key Responsibilities:
✔ Create and maintain Master Study Schedule for all Cliantha sites.
✔ Coordinate with HODs to ensure project milestones are met.
✔ Monitor critical path activities and resolve interdependencies.
✔ Ensure compliance with FDA, GCP, and regulatory standards.
✔ Assist in report compilation (CS-BE, FDA tables).
Eligibility:
- Education: B.Pharma / M.Pharma
- Skills: Strong English communication, BA/BE study experience (mandatory).
2. Medical Writer
Experience: 2-6 years | Salary: ₹3-6 LPA
Key Responsibilities:
✔ Design and prepare protocols, case report forms (CRFs), and informed consent documents.
✔ Coordinate with investigators, biostatisticians, and sponsors for approvals.
✔ Translate English to Gujarati for consent forms.
✔ Ensure compliance with FDA, GCP, and ICH guidelines.
Eligibility:
- Education: B.Pharm, M.Pharm, Pharm.D
- Skills: Experience in medical writing, regulatory submissions, and protocol drafting.
Why Join Cliantha Research?
✅ Work with a globally recognized CRO.
✅ Career growth in clinical research & regulatory affairs.
✅ On-site (Ahmedabad) opportunities with structured training.
How to Apply?
Application Link For Global Project Manager (BA/BE Studies)
Application Link For Medical Writer
