Suyen Go

Clinical Project Manager @Doheny Eye Institute

Los Angeles, CA, US
EMAILS
s•••@doheny.org
MOBILE NUMBERS
+16•••••••26

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WORK HISTORY

Jun 2021 — Present

Clinical Project Manager @Doheny Eye Institute

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Manage full-scope ophthalmic clinical trials (phases from start to finish including study setup, execution, and archival. Manage cross-functional clinical trial operations including project planning, study metric and progress tracking, document and change control, and EDC configuration and monitoring Liaise between pharmaceutical companies, contract research organizations, and the cross-functional team at Doheny Eye Institute to ensure that clinical trials are delivered on-time, according to contract and study documentation, and in adherence to GCPs, SOPs, FDA/ICH Guidelines, and clinical protocol Negotiate contracts, plan and track budgets throughout the course of each study, perform budget reconciliations, invoice each study and verify adherence to financial terms of applicable contracts Perform risk prioritization and impact assessment, issue and address protocol deviations and non-conformances, plan and execute CAPAs as needed, maintain study audit readiness

EDUCATION

2013 — 2017

Ira A. Fulton Schools of Engineering at Arizona State University

Bachelor’s Degree, Bioengineering and Biomedical Engineering

SKILLS

Event PlanningGeneticsHistologyNeuroscienceLabviewQuality SystemMimicsGenetic EngineeringNeuroanatomyArduinoMicrosoft WordCrisprData AnalysisTissue CultureU.s. Food and Drug Administration (Fda)RMathcadAnsysLeadershipTeamworkResearchFda GmpStem Cell ResearchMatlabMicrosoft OfficeSalesMicrosoft PowerpointHepatologyOptogeneticsTeachingCold CallingCustomer ServiceSocial MediaCell CulturePublic SpeakingCell BiologyCustomer Relationship Management (Crm)NeuropathologyPowerpointMicrosoft Excel

ABOUT SUYEN GO

Clinical Trial Manager with strong Clinical Operations and Project Management experience for ophthalmic clinical trials at Doheny Eye Institute, a leading center for vision research and care. I plan, implement, and monitor multiple clinical trials for various eye diseases, working with Sponsors, CROs, clinical teams, and cross-functional staff.The trials I manage are varying in phase and size, and I have skills in clinical research, timeline management, contract negotiation, budgeting and financial forecasting, change control, document authoring, risk prioritization, SDLC, EDC and more. Please feel free to reach out with any questions.

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