- 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.
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