UC Davis 2013-2014 CRC Basic 2.0 Training Program
CTSC Clinical Trial Resources is pleased to announce our 2013-2014 CRC Basic 2.0 training program.
CRC Basic 2.0 is designed for investigators and staff who wish to improve their competency in the field of clinical research management. Upon completion of the Basic 2.0 program, participants will be prepared to coordinate clinical research projects from study initiation to close out in compliance with Good Clinical Practice (GCP) Guidelines. The course specifically addresses local implementation of GCP in performing day-to-day clinical research activities at UC Davis.
The CRC Basic 2.0 training program is organized into 8 modules (listed below). Each module consists of a 60 minute lecture, a 45 minutes hands-on training/exercise (e.g., mock clinical trial budget analysis and serious adverse event report). Certificates of completion are issued after completion of the post-module on-line quizzes and eligible for a 3.0-hour continuing education credit (for each module) towards CNE, SoCRA, or ACRP.
Participants can sign-up for the individual modules or the entire course. Those completed the entire course will receive the Certificate of Completion of CRC Basic 2.0. Each module is limited to 20 participants.
9/13/2013 Introduction to GCP. Miles McFann, IRB Outreach and Education Officer, UCDMC IRB Administration
10/11/2013 Investigational Drug Management. Joyce Lee, Pharm D., Investigational Drug Services
11/8/2013 Study Management. Caren Galloway, CRC, Orthopedic Surgery, UCDMC
01/17/2014 Clinical Trial Budgets. Julie Calahan, Clinical Trial Budget Analyst
02/21/2014 Adverse Events and Protocol Deviations. Elizabeth Mathis, CRC, CTSC
03/21/2014 IRB Submissions. Miles McFann, IRB Outreach and Education Officer, UCDMC IRB Administration
04/18/2014 Medicare Coverage Analysis. Suzan Bruce, CPC, CTSC
05/16/2014 Study Documentation. Elizabeth Mathis, CCRP, CTSC
06/20/2014 Informed Consent Bootcamp. Elizabeth Mathis, CCRP, CTSC; Kate Marusina, PhD, MBA, Manager, Clinical Trials
Questions? Contact Kate Marusina, email@example.com
About CTSC Clinical Trials Resource Group
We provide broad range of support services to the UC Davis Research Community, streamlining the path to regulatory approval of human subject protocols and maintaining the regulatory compliance for the duration of the study.
Services We Offer
1. Logistical support to clinical research protocols
2. Education and training of investigators and staff
3. Clinical trials monitoring
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