Sarah Gilroy

Senior Director, Clinical Site Operations @Neumora

Denver, CO, US
EMAILS
s••••••••@neumoratx.com
MOBILE NUMBERS
+91 *********19

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WORK HISTORY

Feb 2025 — Present

Senior Director, Clinical Site Operations @Neumora

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EDUCATION

1992 — 1996

University of Puget Sound

Bachelor of Arts (BA), Psychology

SKILLS

Data ManagementClinical OperationsClinical MonitoringClinical Trial Management System (Ctms)IrbCROGood Clinical Practice (Gcp)Clinical ResearchClinical DevelopmentIch-GcpVendor ManagementPancreatic CancerRegulatory AffairsBiotechnologyCRO ManagementGcpBladder CancerClinical TrialsCrf DesignInstitutional Review Board (Irb)Electronic Data Capture (Edc)EdcCtmsPharmaceutical IndustryFdaPulmonary HypertensionProstate CancerRegulatory RequirementsRegulatory SubmissionsOncologyProtocolClinical Study Design

ABOUT SARAH GILROY

Resourceful Clinical Research Professional with extensive experience in cross-functional team management from study design and start-up through regulatory submission. Highly adept in site and vendor identification, selection, and management. Expertise in developing study documents including protocols, ICFs, CRFs, monitoring tools, study specific processes/plans and RFPs. Comprehensive knowledge of regulatory requirements and ICH/GCP guidelines. Regarded for the ability to work well under pressure and manage multiple priorities. Utilize strong organizational and communication skills to clarify issues, advocate solutions, and build relationships with internal and external partners.Specialties: Therapuetic Experience: bladder cancer, breast cancer, colon cancer, lung cancer, pancreatic cancer, prostate cancer, pulmonary arterial hypertension, pulmonary hypertension

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