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Needham, MA, February 17, 2012 — Barnett International announced today the launch of fourteen new in-person and web-based courses. In addition to updating its current portfolio of offerings for of the 2012 calendar year, these new courses were added to further serve the constantly evolving training and educational needs of global clinical research professionals today.

New In-Person Courses:

  • The Clinical Data Management (CDM) Component of Clinical Trials for the Non-CDM Professional
  • Developing CRAs as Study Managers

New Web-Based Courses:

  • Design Considerations for GCP Training Programs
  • Going Independent: Fundamentals for Independent Consultants
  • How Sites Can Own the Study Process
  • Investigator Selection Criteria and Strategies for Investigator Qualification
  • Proposed Changes to DHHS Human Subjects Research Protections: Enhancing Subject Protection and
    Reducing Ambiguity for Investigators
  • Quality Risk Management in Clinical Trials and Pharmacovigilance
  • Re-Inventing Investigator Meetings: From “Bore and Snore” to “Engaging and Effective”
  • SOP Lunch and Learn Web Seminar Series
  • Strategies for Protocol Operationalization and Adherence
  • To Rejuvenate the Study or Not: The “Who, What, When, Where, and How” of Study Rejuvenation Meetings
  • Tools for Trainers: Clinical Research Job-Aids and Checklists

“Barnett’s new courses address key issues and identified training needs frequently requested by our clients,” said Naila Ganatra, GM of Barnett International. “We are particularly excited about our new courses for training professionals, which are specifically designed to further our shared goal of providing meaningful training opportunities that are hands-on and practical.”

Barnett’s new courses are available as both in-person and web-based training options, providing a high degree of flexibility for learners. To view Barnett International’s catalog of training courses, download the 2012 catalog at  For our full portfolio of training opportunities, including industry publications, on-site training programs, eLearning programs, and other consulting opportunities, please visit:

About Barnett International: Founded in 1979, Barnett International is widely recognized for its superior consulting services and its targeted education and training programs. Barnett helps clients get the most out of their research and development dollars by managing change effectively, improving organizational performance, and enhancing staff knowledge. The Barnett approach is a unique combination of strategy development and practical, hands-on implementation. The "Barnett Difference" is evident in our deep understanding of the clinical research process and in the rapid and tangible performance improvements we deliver.

Barnett’s new courses are available as both in-person and web-based training options, providing a high degree of flexibility for Learners.

For more information, contact Customer Service at (781) 972-5400


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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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 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)