Cliantha Research is a leading global Contract Research Organization (CRO) specializing in Bioavailability (BA), Bioequivalence (BE), and clinical research services. With a strong reputation (โญ 4.0+ ratings), Cliantha offers end-to-end clinical trial solutions, regulatory compliance, and cutting-edge research in pharmaceuticals.
๐ Location: Ahmedabad, India
๐ Industry: Clinical Research / Contract Research
Job Openings at Cliantha Research
1. Global Project Manager (BA/BE Studies)
Experience: 1-2 years | Salary: โน2-3.5 LPA
Key Responsibilities:
โ Create and maintain Master Study Schedule for all Cliantha sites.
โ Coordinate with HODs to ensure project milestones are met.
โ Monitor critical path activities and resolve interdependencies.
โ Ensure compliance with FDA, GCP, and regulatory standards.
โ Assist in report compilation (CS-BE, FDA tables).
Eligibility:
- Education:ย B.Pharma / M.Pharma
- Skills:ย Strongย English communication, BA/BE study experience (mandatory).
2. Medical Writer
Experience: 2-6 years | Salary: โน3-6 LPA
Key Responsibilities:
โ Design and prepare protocols, case report forms (CRFs), and informed consent documents.
โ Coordinate with investigators, biostatisticians, and sponsors for approvals.
โ Translate English to Gujarati for consent forms.
โ Ensure compliance with FDA, GCP, and ICH guidelines.
Eligibility:
- Education:ย B.Pharm, M.Pharm, Pharm.D
- Skills:ย Experience inย medical writing, regulatory submissions, and protocol drafting.
Why Join Cliantha Research?
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Work with a globally recognized CRO.
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Career growth in clinical research & regulatory affairs.
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On-site (Ahmedabad) opportunities with structured training.
How to Apply?
Application Link For Global Project Manager (BA/BE Studies)
Application Link For Medical Writer
