I have spent my entire career working in clinical research at 3 major medical device firms. My professional experience was first focused on clinical data management building case report forms, reviewing clinical data as per specifications defined by the study team, creating reports to govern clinical studies and managing training and access to clinical study databases. Since 2013, I have managed all aspects of clinical study execution from study start-up to close out. Those tasks include project management of study deliverables, protocol development, site initiation, contract negotiation, on-site monitoring, review of medical publications, and writing clinical study reports to support regulatory submissions.