Kymberli Schrock
Clinical Research Associate Ii @IQVIA
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WORK HISTORY
Clinical Research Associate Ii @IQVIA
EDUCATION
Arapahoe High School
High School
Colorado State University
Bachelor of Science (BS), Major: Health and Exercise Science
ABOUT KYMBERLI SCHROCK
Clinical Research Associate (CRA) II with over 5 years of experience in the Clinical research and pharmaceutical industry in different positions including Clinical Research Associate, Senior Local Remote Site Monitor (RSM-L), and Lead Professional Research Assistant PRA). As a CRA II works on 3 clinical trials in the Neuroscience therapeutic area and gained significant experience in adult Narcolepsy Type I and Type II. Performs on-site SIV’s, Booster Visits, IMV’s, and remote SIV’s with Centralized Monitoring including: 100% or reduced Source Data Verification (SDV), Adaptive and Intelligent Monitoring (AIM) sampling, Event Triggered Real Time Review (ETRTR), and Key Risk Indicators (KRI’s). As a Senior RSM worked on 4 Clinical trials in Allergy, Ophthalmology and Nervous System Therapeutic Areas. Performed Feasibility assessments. Conducted regularly scheduled site management contacts with sites to support the execution of their study responsibilities. Documented and helped follow to resolution, issues and findings noted during SMC’s. Experience from initial IRB submission, start-up, activation, enrollment, database lock (DBL) and close-out. Participated in the RSM-L Peer Mentor Program where provided an experienced contact for new RSM-L’s to offer support and be a resource for everyday tasks during onboarding and their time as an RSM. Assisted in orienting and guiding new RSM’s to become more familiar and confident with processes. As the Lead PRA, worked on 15 Clinical trials in the Cardiovascular Therapeutic Area that were both Sponsor and Investigator initiated. Provided guidance, support and leadership for other PRAs on the team. Performed administrative and regulatory tasks and was responsible for entirety of study coordination from initial IRB submission, start-up, activation, enrollment, DBL and close-out. Experience with Stem Cell therapy. Experience using different clinical and/or client specific systems for trial management such as CTMS, eTMF, EDC, IVRS, EMR, IRB, eDiaries, and billing and imaging systems.
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