Full Time
Medical Monitor
Cliantha Research
Ahmedabad
₹18 LPA
Posted 05/01/2026
About the Role
Role & Responsibilities
• Provide medical oversight for clinical trials
• Review safety data and adverse events
• Ensure protocol compliance
Qualification
• MD Pharmacology
Experience
• Fresher
Skills
• Safety evaluation, clinical judgment, documentation
About the Company
Cliantha Research is a global CRO conducting multinational clinical trials.
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