Deirdre Cochran
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Executive Summary
Deirdre Cochran is a highly experienced professional with 14.5 years of work experience in the clinical trial field. She has a strong background in pcr, cell culture, western blotting, molecular biology, and biochemistry. Currently, she is working on start-up activities for new clinical trials, including IRB submissions, 1572, FDF, and PSP collection and consent form writing. Deirdre has expertise in regulatory, eIRB, Advarra IRB, WCG IRB, Sterling IRB, Shared Investigator Platform (SIP), Consent Form Writing, Clinical Trial Coordination and Management, Oncology, Data Management, eCRF, GCP, ICH
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Providence Health & Services
study start-up regulatory coordinator ii ccrp
study start-up regulatory coordinator ii ccrp
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