Roles & Responsibilities
• Manage volunteer registration and screening processes
• Coordinate with diagnostic laboratories for clinical reports
• Conduct and support the informed consent process for study volunteers
• Perform volunteer enrolment activities as per study protocol
• Monitor volunteers throughout the study duration
• Support investigational product administration activities
• Manage volunteer discharge activities as per protocol requirements
• Compile, maintain, and update study documents and Trial Master File (TMF)
Qualification
• B.Pharm / M.Pharm
Experience
• 2–3 years of relevant experience in clinical research or clinical pharmacology studies
No. of Positions: 07
Skills
• Good understanding of clinical trial processes and GCP guidelines
• Strong documentation and coordination skills
• Attention to detail and ability to follow protocols
• Effective communication and teamwork skills
About the Organization
Jeevan Scientific Technology Limited is a leading life sciences services company offering integrated solutions in clinical research, bioavailability and bioequivalence studies, regulatory, and quality services, supporting global pharmaceutical and biotech organizations.
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