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conferenceseries
.com
Volume 7, Issue 5 (Suppl)
J Clin Trials, an open access journal
ISSN:2167-0870
Clinical Trials 2017
September 11-13, 2017
September 11-13, 2017 San Antonio, USA
4
th
International Conference on
Cl inical Tr ial s
Re-inventing the entry-level clinical research coordinator
Lauren E Ballina
Clinical Research Fastrack, USA
T
he varying level of knowledge, competency, and professionalism of clinical research coordinators at the site level is
problematic in clinical research. The role of clinical research coordinator (CRC) is a technical position requiring working
knowledge of ICH GCP and the code of federal regulations. CRCs are required to collect and document data appropriately
and accurately. Their work can have direct impact on the efficiency and quality of a trial. Of 60 current clinical research
professionals surveyed, 4 (7%) reported purposefully seeking a position in clinical research. The remaining 56 reported that
they fell into clinical research and stayed because the field is so rewarding. All reported on the job training in their entry-
level position as inconsistent and incomplete. Many felt overwhelmed in their first position and that experience and mistakes
have been their best teachers. Clinical Research Fastrack (CRF) has sought to standardize entry-level training for CRCs. By
delivering a robust curriculum focused on ICH GCP, code of federal regulations, protocol, good documentation practices,
adverse events, protocol deviations, clinical trial operations, participant recruitment and retention, responsibilities of study
teammembers including PI, informed consent, and research skills all coupled with a hands-on internship at a clinical trial site,
CRF is re-inventing the entry-level CRC. Through training standardization and utilizing an innovative educational approach
of massed practice CRF is helping transform the role of coordinator to a profession and not just a job. As more well-trained
individuals obtain positions in the field, the industry as a whole will benefit.
Biography
Lauren E Ballina has a degree in Psychology and Master’s in Biomedical Science. She is a SOCRA certified Clinical Research Coordinator. She coordinated clinical
trials at the University of North Carolina at Chapel Hill and The Mayo Clinic Arizona. She is currently the National Program Director at Clinical Research Fastrack.
She is a natural educator and passionate about making the field of Clinical Research a respectable profession and not just a job.
lauren@clinicalresearchfastrack.comLauren E Ballina, J Clin Trials 2017, 7:5 (Suppl)
DOI: 10.4172/2167-0870-C1-019