Jennifer Ebner
About Jennifer Ebner
Jennifer Ebner is a Clinical Trials Safety Specialist with extensive experience in clinical research and safety management. She has worked with various organizations, including Nuvaira, Inc., Medtronic, and CVRx, and holds a Bachelor's degree in Health Science - Pharmaceutical Sciences from Drake University.
Current Role at Nuvaira, Inc.
Jennifer Ebner serves as a Clinical Trials Safety Specialist at Nuvaira, Inc. since 2021. In this role, she supports the collection and tracking of required regulatory documents from global Clinical Centers. She utilizes Clindex and Documentum systems to ensure compliance and efficiency in the documentation process.
Previous Experience in Clinical Safety and Administration
Prior to her current position, Jennifer worked at Advanced Clinical as a Clinical Safety Specialist from 2019 to 2021. She also held various roles in clinical administration, including Clinical Study Specialist I at CVRx from 2016 to 2017 and Clinical Study Support Coordinator at Medtronic in 2017. Her experience includes conducting internal audits of site files and master clinical files.
Educational Background in Health Science
Jennifer earned her Bachelor of Science degree in Health Science - Pharmaceutical Sciences from Drake University, where she studied from 2010 to 2014. This educational foundation has equipped her with the knowledge necessary for her roles in clinical trials and safety.
Research and Internship Experience
Jennifer has a diverse background in research and internships. She worked as a Research Assistant at Drake University from 2012 to 2013 and completed internships at UnityPoint Health and BridgePoint Medical, Inc. in 2013. These experiences contributed to her understanding of clinical research processes.
Skills in Clinical Research and Documentation
Jennifer possesses skills in processing patient reimbursements and quarterly Case Report Form (CRF) reimbursements. She is experienced in navigating electronic medical records and applying inclusion/exclusion criteria to candidate pools. Additionally, she conducts reviews of CRFs in study databases such as Oracle Clinical and Argus.