Sara Curtiss

Clinical Trial Manager @Advanced Clinical

Nashville, TN, US
MOBILE NUMBERS
+91 *********19

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WORK HISTORY

Nov 2024 — Present

Clinical Trial Manager @Advanced Clinical

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Nashville, TN, US

Manage and coordinate hematology and trauma clinical research trials for the United States and Canada• Coordinate study start-up, site activation, database lock and study close-out with monitoring teams and global management • On assignment with CSL Behring, LLC under an FSP model, Lead Clinical Site Ambassador • Experienced with PowerBI, Veeva Clinical Vault CTMS, Veeva Quality Vault, Veeva TMF, Smartsheets

EDUCATION

2004 — 2008

Allegheny College

Bachelor of Science (B.S.), Biology, General

2007 — 2008

James Cook University

Biology/Biological Sciences, General

2008 — 2009

University of Pittsburgh

Master of Arts (MA), Secondary Education and Teaching

SKILLS

TeachingResearchCurriculum DevelopmentTutoringLeadershipTrainingClinical ResearchBiologyOrganization SkillsSite ManagementIch-GcpInstructional DesignSciencePublic SpeakingEducationProgram DevelopmentWritingData ManagementGcpStaff DevelopmentCurriculum DesignClinical MonitoringCRO

ABOUT SARA CURTISS

I have a decade of experience within the pharmaceutical clinical research world in trial management, monitoring and quality assurance. I currently work as a Clinical Trial Manager under an FSP model for the United States and Canada.I have worked as a Quality Assurance GCP auditor with Medpace and as a Senior Lead CRA and Local Study Manager with AstraZeneca and Covance. I have experience running studies in the fields of metabolic diseases (diabetes and NASH), cardiovascular heart failure, endocrinology, respiratory, infectious diseases (such as COVID-19), and hematology research.

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