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:
- Flexible schedule
- Paid sick time
- Paid time off
Experience:
- Clinical Research Associate: 1 year (required)