Lisa MulcahyPrincipal Consultant
Mulcahy Consulting, LLC
Lisa Mulcahy is aversified clinical research professional with more than 25 years of experience in the pharmaceutical research industry. Her current focus is clinical research document management, tying all previous work experiences together to develop and implement high-quality document management processes focusing on the Trial Master File, and QC of TMF documents. She has extensive experience in conducting clinical trials, evaluating quality within clinical trial processes, and the management of documents created during the conduct of clinical trials, all according to ICH-GCP Guidelines.