Clinical Research Associate
7 hours ago
Key Responsibilities
- 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.
Pay: ₹15,851.18 - ₹20,802.54 per month
Schedule:
- Day shift
Work Location: In person
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