Clinical Research Coordinator

5 days ago


Pune Maharashtra, India Statistical Insights Full time

**Responsiblities**:

- Provide clinical study start up expertise.
- Assist Lead CRA in the preparation of IRB submissions including the review of the sitespecific informed consent and assent forms
- Track IRB submissions
- Collect, review, and process essential documents and identify issues that site needs to address.
- Communicate to site the updates needed to the essential documents as needed.
- Lead or support set-up and maintenance of TMF
- Assist and/or participate in planning and conduct of Investigator’s Meetings as necessary.

**Salary**: ₹16,000.00 - ₹39,784.68 per month

**Benefits**:

- Internet reimbursement

Schedule:

- Day shift

Supplemental pay types:

- Performance bonus

**Education**:

- Bachelor's (preferred)



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