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

Perks:

- Flexible schedule
- Paid sick time
- Paid time off

Experience:

- Clinical Research Associate: 1 year (Required)

Work Location: In person

📌 Clinical Research Associate (Delhi)
🏢 PrimEdge Workforce Solutions
📍 Delhi