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Managing CRAs to Improve Study Outcomes March 2010

Course Description 

Monitoring of a clinical trial is a required activity completed by sponsors of FDA regulated research that significantly affects the outcomes of product development and approval. Sponsors effective management of CRAs’ performance is essential. Promoting improvement in overall and individual monitoring is important. Performance Management and Improvement is a Science involving logical processes and applications.  This course will present the concepts of Human Performance Improvement (HPI) and apply it directly to the management of the CRA to promote improvements. The HPI CRA Management Model will be presented and applied in case scenarios for better understanding.  

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Learning Objectives 

  • Define the Human Performance Improvement Model 
  • Recognize an HPI CRA Management Model 
  • Apply the model into current practice: proactive CRA management 
  • Apply the model into current practice: managing CRA performance issues 
  • Analyze case scenarios 

Who Should Attend 

  • Project Managers 
  • Lead CRAs 
  • CRA Managers 

Instructor 

Sandra “SAM” Sather, MS, BSN, CCRA, CCRC 

Click here for complete trainer biographies 

Course Length Time 

2 hours; 12:30 – 2:30 p.m. Eastern 

Course Dates 

March 26, 2010 

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)