Job Description:
Preparing & reviewing SOPs
Reviewing protocol and related documents
Identifying potential Investigator sites
Maintaining the database of the Investigator site
Conducting site selection, initiation
Conducting close-out visits
Training investigator and related site staff on the study protocol
Responsible for vendor selection
Responsible for ensuring the clinical trial supplies at the sites
Accountability of clinical trial supplies
Reviewing the source data and maintaining the integrity and quality of the trial
Reporting of any event to the superiors in case of non - compliance.
Preparing and circulating the monitoring reports
Ensuring the observations are closed and adhering to the protocol requirements
Coordinating with other departments like CDM, statistics, and QA to ensure all the data-related
observations are closed
Reviewing of reports
Pay: ₹30,000.00 - ₹60,000.00 per month
Advantages:
Versatile schedule
Paid sick time
Paid time off
Experience:
Clinical Research Associate: 1 year (required)