Kelsey Beller
Study Project Manager i @AbbVie
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WORK HISTORY
Study Project Manager i @AbbVie
Responsible for executing one or more elements of clinical studies in compliance with quality standards (ICH/GCP, Global Regulations, and AbbVie policies and procedures).Supports in leading the cross functional study team:o -Supports the preparation of Clinical Study Team meetings (Agenda/Minutes)o -Responsible for regular updates to the cross-functional team and stakeholders on study status; ensure our CTMS is up to dateSupports the development of the clinical study blueprint/protocol and associated systems and documents (Informed consent forms, eCRFs, IRT, CSR)Supports the vendor selection, scope development, management and oversight of external vendors in compliance with AbbVie’s processes and procedures and the applicable regulations.Responsible for generating the study related training for the study team, study sites, and vendors for assigned studiesProactively identify and resolve and/or escalate study related issuesParticipates in process improvement initiatives
EDUCATION
The University of Kansas
Bachelor's degree
ABOUT KELSEY BELLER
Study Project Manager I at AbbVie
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