Regulatory Associate San Antonio, TX

Written By Dan Sfera

Regulatory Associate
San Antonio, TX
100% on-site, no remote flexibility
Permanent

• Will ensure timely and accurate submission of regulatory/IRB documents for new and ongoing studies
• Day-to-day responsibilities will include site compliance with SOPs, Sponsor/CRO requirements, FDA/ICH guidelines and GCPs.
• 1-2 years Regulatory Submissions experience required

Please submit resume and interest to lsummers@greenkeyllc.com

Dan Sfera
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