Co-founded SP3NW, Washington State University's business incubator for scalable startups. Developed and manage wrap around programs and physical space supporting the launch of over 60 startups.

• Facilitate industry-academic partnerships• Create industry networking opportunities through programming and events• Increase industry visibility by publishing news, events, and job openings• Support and market incumbent workforce training• Facilitate business development opportunities through CRM development and management

• Wrote the trade association manual for incumbent worker training program development and implementation • Developed and implemented an Executive Speaker Series, Intern Boot Camp, and Bioscience Symposium with administrators at Oregon State University

• Review, evaluate and facilitate licensing of university discoveries and intellectual properties• Develop and report technology evaluations and non-confidential summaries• Conduct investigator interviews and support internal and external stakeholder relationships

• Evaluated commercial opportunities for University of Pittsburgh technologies • Identified product-market fit and potential partners/licensees

McGowan Institute, Jan - May 2015• Worked with a team to evaluate business development and outreach efforts for efficacy• Identified and interviewed internal and external collaborating stakeholders• Developed and communicated budget sensitive marketing strategies and collateral to senior leadershipMcKesson, Aug - Dec 2014• Spoke with stakeholders, evaluated development costs and forcasted demand for new market entry• Recommended new market entry strategy with an 190% IRR to local executivesPhilips Home Healthcare, Jan - May 2014• Tracked, aggregated and analyzed process defect data to determine 93% of issues were special causes• Proposed strategic recommendations using Lean/Six Sigma methods to improve error detection processes for Philips Lifeline manufacturing

• 30+ research studies: Prepared regulatory documents including IRB and QI protocols, DUA and MTA applications, and Tissue Utilization• 93% patient consenting rate with no patient complaints: Supervised and trained research staff in regulatory compliance and patient consenting• 16 first or co-authored publications: Managed and analyzed 3 research databases supporting the research efforts of the division of Endocrine Surgery including 3 intra-institutional and 4 inter-institutional collaborations. • Member, University of Pittsburgh Institutional Review Board

• 7 first or co-authored publications: Performed data analysis, manuscript preparation, submission and meeting presentation • Passed 100% of research audits: Prepared regulatory documents including IRB and QI protocols, DUA and MTA applications, and Tissue Utilization• Research expertise: Conducted all stages of study development and implementation

• Conducted study site visits and site management and monitoring activities consistent with FDA regulatory requirements• Shipped study supplies to sites and track and monitor invoicing

• Prepared IACUC, EHS, rDNA, and other regulatory documentation associated with the research study.• Conducted all stages of study development and implementation. • Performed data analysis, manuscript preparation, submission and meeting presentation.

• Clinical front desk administration - scheduling/registration, patient reception/check-in, check-out/follow-up visit coordination and insurance management• Delivered high-level of customer service as the first and last interface with stakeholders including patients/families, referring providers and hospital-based providers.

• Program implementation – Implementated of all lodge based treatment programs• Prepared daily reports, and assist the team in completing treatment reports.• Intervened and assisted in the crisis/interpersonal problem resolution

• Acquired patient vital signs • Documented patient vital signs, observations of patient behavior, complaints, or physical symptoms• Administered basic care and assisted with patient's tasks of daily living.