Clinical Research Coordinator
1 month ago
**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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