GastroLab India Private Limited jobs - Clinical Research Coordination

1. Work on facilitating and coordinating the daily clinical trial activities while playing a critical role in the conduct of the study
2. Schedule and study subject appointments and serve as the patient liaison to the PI and other participating physicians
3. Review and comprehend each assigned protocol, including study proceedings and timelines
4. Work closely with the PI & CRC participants in an integral way in the informed consent process by communicating clearly with potential study subjects about the protocol
5. Coordinate approval of new study agreements and contracts
6. Coordinate and attend sponsor site selection visits, routine monitoring visits, and study close-out visits
7. Complete case report forms and extract data from patient files (source documents) in a timely manner
8. Respond to data clarification requests in a timely manner
9. Attend investigator meetings requiring travel and report pertinent information back to research team members
10. Coordinate with the departments to help ensure that clinical research and related activities are performed in accordance with protocol, SOP, GCP, and applicable regulatory
11. Assist the PI in the development of materials and tools necessary to appropriately train individuals involved in the conduct of the study, like study protocol requirements, schedule of visits, execution of research plan, and maintaining records and other documentation of training