*Not admitted in the District of Columbia, admitted in Massachusetts. Practicing pursuant to D.C. Rule 49(c)(8) under the direct supervision of Lee Rosebush during pendency of application for admission to the District of Columbia.

Responsible for operational oversight of 6 pharmacies in Oregon, Idaho, Utah, Montana, and Colorado.

• Oversees operational performance of Portland, OR and Bend, OR centers, including efficient, effective and high quality delivery of services and patient care. These locations are joint ventures with Legacy Health System.• Ensures patient safety and satisfaction through all operations including pharmacy dispensing operations, nursing, patient registration, and warehouse.• Partners with Regional Director of Sales to drive market development and execute market based sales strategy.• Drives financial performance of all branches through supply chain/inventory optimization, managing controllable expenses, reducing bad debt (claims on hold) and accurate patient registration and onboarding.• Ensures compliance with local and federal regulations, accreditation standards and corporate policies to drive effectiveness and consistency in operations.• Builds a cohesive, service-oriented team through recruitment, training and development, engagement and retention of qualified team members. Maintains a work environment in which staff will succeed and grow in their professional development and contribute to the overall success of Option Care.• Consistently models behaviors that build our culture around the Option Care Core Values of Compassionate Care, Engaged Teams and Quality Results.

• PharmaLabs 503A Sterile/Non sterile compounding pharmacy department P&Lmanagement (staffing model, plan for capital expenditures, annual budget setting,monthly adherence to budget)• Thought leader for inspection readiness, legal/regulatory issues, and operationalchange related to 26 state sterile/non sterile and non resident licenses includingFlorida, California, and Texas• FDA compounding policy expert• Grew PharmaLabs from inception in 2013 to present state of 10,000 prescriptionsmonthly and $9 million in annual revenue.• Reduced COGS and operating expenses as a percent of revenue year over yearthrough process improvement and lean initiatives• 5 direct reports – Pharmacist in Charge, two staff pharmacists, regulatorycompliance officer, and controller among a broader organization of 80 people• Led organization through PCAB accreditation and renewals• PBM Audit experience – reduced express scripts audit chargeback to 3% of original demand.• Edit physician generated study content and marketing content for clinicalaccuracy and alignment with brand look and feel.• Monthly patient portal blog posts to support customer engagement• Hiring, separations, career development, and morale of team• Establish and monitor metrics for each functional role• Department training, cross training, best utilization of resources of team membersin roles• Recruit new physicians into the MenMD network and support onboarding process• Oversaw planning, budget, and buildout of USP 800 compliant ISO 7 negativeroom, and HVAC and ductwork replacement for ISO 7 positive room.• Selection and vendor qualification of 503B pharmacy partners

• Write and design patient education materials across urology/men’s health productlines• Write and design physican and customer sales and marketing materials• 2 direct reports – clinical case managers responsible for triage of patient questionsand adverse event reporting• Concierge consultation service for VIP patients at physician request• Database mining with physician partners to produce data for publication• Approve therapy change request submissions to physicians from case managers• Recruit new physicians into the MenMD network and support onboarding process

• Oversaw operation of customer service/call center sales and clinical departments• Developed, set, and monitored metrics for each position including coaching tomeet business needs and maximize efficiency and productivity• Provided industry and product knowledge to prinicpals to assist with strategydevelopment• Supported Director of Business Development with physician outreach• Primary liaison with all MenMD pharmacy vendors

• Resolved inbound client questions and concerns• Placed scheduled outbound clinical calls• Encouraged product usage and replacement

• Interpreted drug, device, and combination product regulations• Provided regulatory strategy and product development strategy for submissions for topical product and neurosurgery product• Authored the clinical review for FDA submission of Investigational Device Exemption for clinical trials (IDE) and 510(k) premarket notification

• Standard pharmacist dispensing, data entry, and other professional standards • Patient education, drug interaction screening, drug use evaluation• HIV medication adherence and patient outreach• Precept Northeastern University and Massachusetts College of Pharmacy students• Expansion of customer base and revenue through sales activities

Courses taught under appointment:Introduction to International Regulatory Affairs 04/07 – 06/07Production Regulatory Affairs, Good Manufacturing Practices 04/07 – 06/07New Biologic Development: A QA/Regulatory Overview 01/07 – 03/07New Device Development: A QA/Regulatory Overview 01/07 – 03/07New Drug Development: A QA/Regulatory Overview 09/06 – 11/06Food, Drug, and Medical Device Law: Topics and Cases 03/06 – 05/06Pharmaceutical Care Lab 09/05 – 11/05New Drug Development: A QA/Regulatory Overview 09/05 – 11/05Advanced Tutorial in Regulatory Affairs 09/04 – 11/04New Drug Development: A QA/Regulatory Overview 09/04 – 11/04

• Medical information officer through (enfuvirtide) Fuzeon product launch• Didactic education and lecturing for health care providers and sales representatives• Managed clinical training operations and product knowledge for a team of 9 representatives• Initiated proposal before Massachusetts Medical Society and Association of Nurses in AIDS Care to expand pharmacist based medication administration to include enfuvirtide• Product promotion and sales activities• Assist, develop, and encourage participation of regional thought leaders in clinical trials