Project Manager & Medical Writer Jobs – Cliantha Research Hiring Now!
Company: Cliantha Research
Roles: Global Project Manager (BA/BE Studies) & Medical Writer
Location: Ahmedabad, India
Experience: 1-6 years (Freshers not eligible)
Qualification: B.Pharm, M.Pharm, Pharm.D
Job Type: Full-Time
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About Cliantha Research
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.
🔹 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: B.Pharm / M.Pharm | Strong English | Experience in BA/BE mandatory
🔹 2. Medical Writer
- Experience: 2-6 years
- Salary: ₹3-6 LPA
Key Responsibilities:
- ✔ Design and prepare protocols, CRFs, and informed consent documents.
- ✔ Coordinate with investigators and sponsors for approvals.
- ✔ Translate English to Gujarati for consent forms.
- ✔ Ensure compliance with FDA, GCP, and ICH guidelines.
Eligibility: B.Pharm, M.Pharm, Pharm.D | Experience in protocol drafting, submissions
🌟 Why Join Cliantha Research?
- ✅ Work with a globally recognized CRO
- ✅ Career growth in clinical research & regulatory affairs
- ✅ On-site (Ahmedabad) opportunities with structured training
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