- - 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.
- Perform Site Monitoring Visit, Site Close-out visits in accordance with the protocol and other applicable regulatory guidelines including local regulatory guidelines.
- Keep a close association with site for Patient Recruitment, patient follow-up and protocol related activities.
- Act as a communication link between Sponsor and site.
- Attend Investigator's meeting.
- Training of Investigators on Protocol and other applicable regulatory guidelines including local regulatory guidelines.
- CRF retrieval as per the project instructions.