| IRB Administrator, MetroWest, MA |
Author: Cheryl Cormier, CPC
Date: 05-23-05 11:45
If you are in regulatory or IRB Administration with CIP, we have a great job with a solid company just waiting for your skills and experience! Don't miss out on this rare opportunity to share and build on your current skills.
We are seeking a full-time IRB Administrator. You will work with other IRB Administrators to ensure that submitted biomedical research is in compliance with federal regulations. The IRB Administrator is responsible for processing, tracking and filing submissions to the IRB, taking meeting minutes, maintaining IRB files, serving as IRB interface with subjects, investigators and sponsors, and ensuring that continuing review is conducted in a timely fashion. The IRB Administrator will also assist with developing, revising and implementing policies and procedures, as well as serving as an alternate member of the local review board.
Qualifications:
Education: RN, LPN, or BA/BS with experience in clinical trials, knowledge of FDA and OHRP regulations and guidance, strong communication and organizational skills, CIP preferred
Cheryl Cormier, CPC
New Sciences, Inc.
781 749 8344
biojobs@attglobal.net
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IRB Administrator, MetroWest, MA new |
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Cheryl Cormier, CPC |
05-23-05 11:45 |
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