Job Summary
Overall responsibility for study management, responsible for the monitoring of studies in accordance with protocol/ SOPs/ Guidelines.
Responsibilities and Duties
- Perform Site Identification and conduct Feasibility Studies.
- Perform Site Selection Visit, Site Initiation Visits in accordance with the protocol and other applicable regulatory guidelines including local regulatory guidelines.
- Send Follow Up letters to sites and submit Visit Reports to the Clinical Team Leader/ Project Manager as required.
- Keep a close association with site (s) for Patient Recruitment, Patient Follow Up, and protocol-related activities.
- Training of Investigators on Protocol and.
- CRF retrieval as per the project instructions.
- Coordinate and distribute Clinical Study Material to study sites.
- Archival of study documents.
Key Skills
Biotechnology, Microbiology, Upstream Downstream Processing Executive, Production Maintenance, Pharma, study documents, Central Clinical File, local regulatory guidelines
Required Experience and Qualifications
Qualifications: Msc., life science, nursing , B.Pharmacy/M.Pharmacy/ PharmD, M.B.B.S, B.D.S, B.H.M.S, B.A.M.S, etc.) and life science graduates.
Experience:Fresher
Benefits
Pick n Drop
PF
L A Consultancyis one of the dynamic and innovative HR consulting firms based in Chennai, India. L A Consultancy provides comprehensive services in the areas of IT Staffing, Executive Staffing, Temporary staffing, and job placement for varied levels of leading top companies. Our clients include m...