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Real-World Monitoring: Tips for Success and Sanity August 2012

Course Description

The Clinical Research Associate (CRA) position is both demanding and extremely rewarding. This web seminar provides tips and strategies to help the new CRA navigate his/her early years in the profession. Topics ranging from the practical (packing and travel tips) to the philosophical (how to earn trust and credibility) are covered. Participants will also learn how to set the stage for success as a CRA from a veteran monitoring professional.

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Learning Objectives

  • Identify key skills and personality traits for success as a CRA
  • Describe the workflow of a successful monitoring visit
  • List the top five activities required of new CRAs for quality performance

Who Should Attend

  • Clinical Research Associates with two years of experience or less
  • Clinical Research Associate Managers
  • Trainers or those responsible for new Clinical Research Associate on-boarding
  • Individuals pursuing a Clinical Research Associate career

Instructor

Karen L. Gilbert, B.S., C.C.R.A.

Click here for complete trainer biographies 

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

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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

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Live SeminarLIVE SEMINARS

Monitoring Clinical Drug Studies: Intermediate 

Informed Consent Content & Process Requirements for Biobanking Studies 

Auditing Techniques for Clinical Research Professionals 


Web SeminarWEB SEMINARS

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  


PublicationsPUBLICATIONS

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)