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Managing CRAs to Improve Study Outcomes March 2010

Mar 26, 2010
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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 

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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 

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.


Barnett 'Hands-On' In-Person and Web Seminar Workshop Series
Barnett "Hands-On" Workshops are designed to provide intensive, hands-on training in a highly targeted clinical research topic area in a very interactive and engaging learning environment. To view more details and available courses, click here.


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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)