Serve as lead medical reviewer for PAH brands on PRB. Support and attend advisory boards to gain insights for medical affairs initiatives. Assist in training of commercial personnel on medical aspects of promotional material. Collaborate in developing medical/scientific strategy to support marketing initiatives.

◆Respond to written and oral escalated medical information requests received from call centers of multiple clients, across different therapeutic areas. ◆Create standard response letters and conduct periodic review of approved letters. ◆Survey and critically evaluate published literature for inclusion into medical information resources. ◆Develop and maintain database for clients’ products in order to respond to healthcare professional and payer inquiries. ◆Conduct ongoing training of call center staff and field sales personnel on drug products and disease states. ◆Provide medical information booth support at national meetings and conferences. ◆Draft and assist in review of promotional materials for scientific accuracy on client’s PRC. ◆Maintain slide sets in order to respond to payer requests. Present product information to payers on client request. ◆Conduct ad hoc and scheduled literature searches using Ovid and Adis platforms, for adverse event reports of clients’ prescription products. ◆Partner with business development team to draft client proposals. ◆ Manage Development Safety Update Report (DSUR) QC project for client with multiple oncologyproducts.◆Previously worked at Ashfield as Senior Case Manager/Case Manager II, which included the following responsibilities: ◆Triage and process cases with serious and non‐serious events, for cases from United States and rest of world for two large clients with extensive OTC and prescription portfolio, including medical devices. ◆Interact with reporters, affiliates, and clients as necessary to obtain clarification or follow‐up information and assure additional data is appropriately integrated into the ICSR. ◆Utilize MedDRA coding to database events in Argus. ◆Apply knowledge of global regulatory requirements to complex cases to ensure timely submission of accurate and comprehensive reports to worldwide regulatory agencies in accordance with applicable regulations.

◆Prepare presentations and reports in response to drug information questions by Global Strategyand Market Intelligence Department. ◆Evaluate drugs in various stages of clinical development to generate leads for products that may be suitable for manufacture by Patheon. ◆Create company profiles by using EvaluatePharma, PharmSource, and online financial details. ◆Assist with competitor mapping projects using DailyMed and Drugs@FDA databases.

◆Worked in Dr. Tony Hickey's lab and conducted laboratory experiments nebulizing micafungin (Mycamine) and liposomal amphotericin B (AmBisome) to determine their particle size distribution to evaluate their suitability for delivery as an aerosol. ◆Tested several nebulizers to evaluate drug delivery characteristics of each. ◆Developed assays to nebulize liposomal drug formulations.

◆Ensured compliance with all applicable federal and state health and safety regulations to protecthealth & safety of hospital employees. ◆Trained and provided guidance to hospital staff forrespiratory protection, hearing conservation, personal protective equipment, and other OSHAregulations. ◆Conducted walkthrough audits of hospital and clinic areas to assess compliance with Joint Commission Environment of Care Standards and trained staff on these Standards. ◆Member of several Six Sigma projects in various hospital departments to reduce injury rates and improve workplace safety, including a project that reduced lost‐time incidents among foodservice staff by half. ◆Monitored personnel for their exposure to various chemicals, including formaldehyde and ethylene oxide, as well as bioaerosols.