Leadershipo Hired, onboarded, and trained 24 staff as Research Services Professionals (RSPs)o Developed and implemented a training program which included continuing CITI trainings, COI, and reading the Otolaryngology department’s SOPs for the faculty, residents, RSPs, medical students, etc.Contracts:o Routed and guided legal documents through the contracting process to obtain a CTA, CTA Amendments, MTA, or DUA.Finance:o Created and negotiated successful budgets for clinical trials, sponsor funded investigator-initiated studies, and NIH funded studies.o Communicated with study teams to invoice sponsors, and pay invoices.o Monthly gift card and petty cash audits with the custodians of those accounts.Regulatory:o Managed over 220 investigator-initiated studies and clinical trials.o Worked on over 30 FDA regulated device and drug clinical trials and investigator-driven clinical studies.o Preformed self-audits and quality checks of our full board studies and clinical trials.o Successfully organized inspections and reviews on studies from the CU Cancer Center and Clinical Research Support Center.o Worked with several IRBs: COMIRB (our local IRB), WIRB, ADVARRA, Alpha and IRBs that COMIRB has ceded to.o Wrote, submitted, and amended study documents: IRB applications, protocols, consent/assent forms, interview guides, questionnaires, CRF’s/DCF's, recruitment materials, and source documents, etc.Data collection:o Created and maintained REDCap databases for data collection, analysis, and storage.Otolaryngology’s Research Department:o Wrote and edited our departmental Standard Operating Procedures.o Developed relationships with clinicians, clinic staff, and monitors/sponsors to facilitate study efforts and have successful trials.o Developed relationships with staff around Anschutz to facilitate research and promote Otolaryngology.

Study Visits:o Recruited, screened, scheduled and consented participants into research studies with challenging inclusion/exclusion criteria.o Choreographed study visits for clinical trials and investigator studies by communicating with participants to address concerns and collect data.o Organized and entered data into paper files and electronic databases, i.e., DataLabs, iMedidata Rave, Clintrack, iMedNet, Bioclinica, Florence, Veeva.o Shipped blood, urine, and tissue samples; received investigational product and devices.o Created and maintained REDCap databases for data collection, analysis, and storage.o Supervising a staff of professional research assistants. o Taking clinical trials from beginning to end including weighing their feasibility, creating and submitting applications to the IRB, coordinating study staff and booking rooms, recruiting, running participants through the trial, working with hospital billers, closing studies.

www.whri.org• Worked on a clinical trial for a Pertussis vaccine in pregnant women. Women and their infants were followed the last 6 weeks of their pregnancy and for 18 months post-partum with cord blood samples, mother and baby blood samples, and breast milk samples.• Worked on investigator-driven clinical research on vaginal health in samples of women who were: healthy normal, pregnant, and those with recurrent Bacterial Vaginosis• Wrote, submitted, and amended study documents: ethics applications, protocols, consent forms, CRF/DCF’s, and recruitment materials.• Recruited, screened, and consented participants into research studies with challenging inclusion/exclusion criteria• Liaised and developed relationships with clinicians, their staff, and monitors to facilitate recruitment efforts.• Communicated with participants to address concerns, coordinated visits, and collected data• Organized and entered data into paper files and electronic databases • Created and maintained REDCap databases for data collection, analysis, and storage• Wrote and distributed weekly recruiting reports to sponsors and annual reports for grant-funded studies regarding recruitment efforts, study progress, and knowledge translation.

www.scaleart.ca• Office management: organized calendars and meetings, maintained timelines/deadlines• Managed the company finances: budgeting, account receivables, account payables, and payroll• Drafted correspondence and documents, editing, proofreading, note taking• Marketing: researched new clients and distributed marketing documents• Software/social media used: Quickbooks, Microsoft Office 2007 for Windows and Mac (Word and Excel), LinkedIn, Google Calendar and Docs

www.earlylearning.ubc.ca• Assisted in developing and running the day-to-day operations• Organized and maintained records • Communicated and coordinated with stakeholders in a timely and professional manner • Marketing: wrote and distributed information packages, gave educational presentations• Wrote and implemented complex study protocols• Trained research assistants and volunteers • Software used: Microsoft Office 2007 (Word, Excel, Outlook, Power Point), Google Calendar and Docs, nVivo, SPSS, ACCESS, Zotero

In this position I transcribed and coded 15 hours of focus group interviews and wrote reports for the Ministry of Healthy Living and Sport as well as the BC Health Authorities regarding the status of children's dental services in the province.

Under the direction of Dr. Veronica Strong-Boag, I completed historical research projects.