Experienced Senior Clinical Trial Associate with over 15 years of experience in clinical research seeking a challenging position in the pharmaceutical & biotech industry. Extensive experience in clinical trial site management; investigator management; regulatory document review; patient information tracking, handling & processing; site and vendor payment tracking & processing; project management activities such as taking meeting minutes, preparing agendas for meeting minutes and maintaining study status trackers. Motivated to learn, grow and excel in the Biotech industry. Experience with various databases such as CCT (Clinical Cost Tracking) - financial accounting and payment systems & EDC (Electronic Data Capture) - tracking site-specific patient information. Knowledge of ICH/GCP (International Conference on Harmonization (ICH) - Good Clinical Practice (GCP).
Communicate effectively with discretion & professionalism and organize time and tasks skillfully. Took a career break to attend to family and complete bachelor's degree; have kept up with professional skills during this time.
Auditing Techniques for Clinical Research Professionals; presented by Barnett International, July 2009, San Francisco, CA. •Attended a class for Intermediate CRA course; presented by ACRP (Association of Clinical Research Professionals), October 2008, Houston, TX.
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