10-Week Clinical Research Associate (CRA) On-Boarding Program

Upcoming Courses
Course #: BI11515
June 6 - August 22, 2014
8:30 AM - 11:30 AM Eastern

Friday mornings. No class July 4 or July 11.

Take advantage of our $1,695.00 price by registering early!
* After May 5, costs are $1,895.00.

10-Week CRA On-Boarding Logo 

Course Description

The online 10-Week Clinical Research Associate (CRA) “on-boarding” training course is appropriate for individuals who have less than two years experience as a Clinical Research Associate. The course provides practical, hands-on training as it relates to the CRA job function, and covers core sponsor and research site activities that promote the successful monitoring of studies for both drug/biologic and device trials. The course follows an ICH/ISO global GCP framework, and covers how to identify specific country requirements, making it appropriate for both US and global audiences. Core Good Clinical Practice (GCP) skills are reinforced through a combination of activities, including lecture, case studies, and scenario review, as well as application-based homework assignments.

This course is built on Barnett’s deep in-person CRA training experience and is designed for “on-boarding” of individual new hires or entire teams. If you are a CRA manager or human resources professional responsible for the orientation and training of one new CRA or 100, this course provides a convenient, cost-effective, comprehensive, and interactive training method. You’ll have the peace of mind knowing that you are training your new hires to the highest industry standards.

The resources required to take this on-line course are already at your fingertips - an Internet connection and a phone. After registering, you will receive an email confirmation that provides you with the Web Seminar link and audio connection information.

Before the class starts, you will receive your class books and reference guides. During the live Interactive Web Seminar, you will be able to ask questions and provide feedback. You will be required to pass both a mid-term and a final in order to receive accreditation CEUs. Upon completion, training certificates will be provided to all participants and accreditation CEUs will be requested.

Learning Objectives

  • Module 1: Drug Development Process, Good Clinical Practice (GCP) and Clinical Research Team Roles and Responsibilities
  • Module 2: IRB, Clinical Study Protocol Elements and Amendments
  • Module 3: Informed Consent
  • Module 4: Investigational Product Accountability
  • Module 5: Safety Definitions and Reporting Requirements
  • Module 6: Source Document Verification
  • Module 7: Monitoring the Study
  • Module 8 and Module 9: Monitoring Visit Reports and Contact Reports
  • Module 10: Regulatory Compliance and Quality Assurance: Audits and Inspections

Who Should Attend

  • Clinical Research Associates with less than two years experience – In-house or Field-based
  • Those currently working in the industry in a different role and seeking to change roles
  • The course is also ideal for “on-boarding” of individual new hires or entire teams (individual registrations required)

NOTE: This course is for individual registrants only and does not allow for group training.


This course will be taught by one of the following instructors: 

Lily Romero, P.A., C.C.R.C.

Jackie Stader, C.O.T, C.C.R.C.

Click here for complete trainer biographies 

Course Length Time

10 weeks for 3 hours each week. Friday mornings, 8:30 – 11:30 a.m. Eastern

Registration Fees

$1,695 by Early Bird Deadline noted in Upcoming Courses section above

$1,895 after Early Bird Deadline

This course is for individual registrants only and does not allow for group training. All participants are eligible for “Certificates of Attendance,” and accreditation, provided that accreditation requirements are met.

Accreditation Information

Barnett International is accredited by the Accreditation Council for Pharmacy Education as a provider of continuing pharmacy education.  Participants will receive 30 hours (3.0 CEUs) of continuing education credit for full participation, including the completion of a pre-test, post-test, and program evaluation.  Barnett International will mail ACPE statements within three weeks of program completion.  ACPE#: 0778-0000-14-015-L01-P. Released: 3/14.

Hold this course at your company! For more information, contact Naila Ganatra at (215) 413-2471. 





LinkedIn twitter Facebook 

On-Demand GCP Refresher Training 

Too busy to attend a course? Our newly-released GCP eLearning course may be your solution!
For details on our scenario-based practical GCP application on-demand course, click here.

GCP for Investigators

Barnett’s scenario-based eLearning course is designed with the busy Principal Investigator in mind.  Based on real-life scenarios encountered by investigative site teams, this highly focused 7-module GCP training is designed to ensure comprehensive understanding of the key components of GCP.

For more details on this scenario-based eGCP program for investigators please click here. 

BARNETT CATALOG The Barnett Catalogue is your comprehensive guide to the myriad live, web, and custom training opportunities offered throughout the year. 

Jan - July 2014 Edition

Winter CatalogDownload Today!  

Blended Curriculum Path for the CRA, CRC, and Project Manager

BCP Cover

Download Today! 






 View Catalog of Offerings   

New Titles added every month! 
Course Alumni Save 50% 


Monitoring Clinical Drug Studies: Intermediate 

Informed Consent Content & Process Requirements for Biobanking Studies 

Auditing Techniques for Clinical Research Professionals 


10-Week CRA & CRC Beginner Program  

Trial Master File (TMF) for Sponsors: Set-Up and Maintenance 

Use of Notes to File in Clinical Trial Essential Documentation 

10-Week Clinical Research Associate (CRA) On-Boarding Program  


2012 GCP Question & Answer Guide Print Edition 

2012 Good Clinical Practice Question & Answer Guide Electronic Edition 

CFR/ICH GCP Reference Guide 2012 (Spiral Bound) 

CFR/ICH GCP Reference Guide 2012 (Perfect Bound) 

PAREXEL's Bio/Pharma R&D Statistical Sourcebook 2012/2013 (Hard Copy)