- Provide collaborative drug therapy management to patients referred to the anticoagulation clinic which includes initiation of warfarin/DOAC, warfarin dosage adjustment, providing education to patients and their families- Reduce adverse effects associated with warfarin therapy and be able to reverse anticoagulation and address management of bleeding events by approved protocols and evidence-based guidelines- Assist physicians in the perioperative management of warfarin or direct oral anticoagulants by designing bridge plans

Staff: ICU/CVU, ED, Internal Medicine, Central- Develop disease-specific, outcome-based therapeutic plans for drug therapyprotocol monitoring (antibiotics, warfarin)- Enter, verify, and send medication orders in Cerner within a timely manner whilestaying incompliance with department/hospital and other regulatory bodypolicies- Research and answer drug information questions for providers- Counsel patients on take home medications upon dischargeProjects: Design and implement Meds to Beds program, Develop protocols for Med Recprogram, Prevention of unnecessary vaccine administration

- Day of Coordinator for Weddings - Specialized in Do-it-Yourself Clientele

- Identify and organize previous Request for Proposal (RFP) answers to help streamline the process for future requests from clients - Review current market facing content regarding Value of Integrated Pharmacy benefits across all pharmacy programs, updating this content and working with marketing to strengthen the message with new data - Support the roll out of the new HMO line of business and provide clinical support for members calling in with pharmacy questions - Assist Pharmacy leadership in analyzing and researching pharmacy cost trends and clinical program opportunities. Drugs of interest: GLP-1, Humira Develop biosimilar switch strategy for Humira - Provide provider support regarding Premera coverage and addressing member issues for the Kinwell network - Serve as the pharmacy expert for multidisciplinary rounds (group B) for complicated patients needing additional support

- Answered phone calls and processed medication orders from medical providers and clients- Built solid customer relationships and delivered exceptional service- Compounded non-sterile medications (capsules, solutions, transdermal, mini-tabs) for human and veterinary clients

- Reviewed package inserts to document trends in dosing based on individual patient factors- Attended presentations to learn about the FDA’s multidisciplinary processes for addressing public health issues involving drugs, biologics, and medical devicesProject:- Reviewed package inserts for 67 New Molecular Entities approved from 2007-2017 in OCP1 (focused on cardio-renal, neurology, and psychiatry drugs)- Studied dose characterization and how patient’s intrinsic factors (age, race, gender, hepatic and renal function) affect dose recommendations

Therapeutic Area: Dermatology- Conducted phase I-IV clinical studies involving biologic, systemic, and topical modes of treatment- Managed data entry and assured quality control of visit documentation/clinic notes, known as source data/document verification (SDV), for 9 clinical trials- Maintained and updated regulatory binders and patient charts for site monitoring visits and regulatory audit visits- Helped supervise 4 undergraduate interns - Worked with principle investigator, site staff, and patients to ensure compliance to study procedures as defined per protocol- Educated patients on proper investigational medication intake and proper diary log record keeping

Prepare chemicals and equipment for weekly experiments in General, Organic, and Inorganic Chemistry Labs

- Designed standard operation protocol templates for product quality testing in labs in accordance to US Pharmacopeia, Japan Pharmacopeia, and European Pharmacopeia standards- Worked under the Quality Assurance supervisor to assess quality and accuracy of submitted paperwork