Location: Delhi – WFH
Employment Type: Full-time
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
Benefits:
- Flexible schedule
- Paid sick time
- Paid time off
Experience:
- Clinical Research Associate: 1 year (Required)
Work Location: In person
