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How Can I Be a Successful CRC

 
  September 11, 2012  
     
 
ComplianceOnline, Online Event
2012-10-10


Why Should You Attend:

With the growth of the Biotechnology industry, Clinical Research Coordinator (CRC) positions are expected to increase by 2016. The CRC is the heart and soul of the trial thus it is important to be well organized and well informed about the role and responsibilities.

This presentation will prepare a coordinator to successfully select a trial, show what to do after you select trails, how to get prepared before the trial start, how to successfully submit to the IRB, maintaining the trial master file, CRFs, post trials activities and much more. All these are done with the primary goal in mind - the rights, safety and well-being of patients prevail over science. Also accurate documentation is a key role of a CRC. You will also how to accurately report, document, handle, store, protect, interpret and verify data.

 Areas Covered in the Seminar:

  • ICH guidelines and Good Clinical Practice (GCP).
  • Types and Phases of Clinical Tril.
  • Role and responsibilities of a Clinical Research coordinator.
  • Key aspects of the role and key players involved in a trial.
  • Role of the Principal Investigator.
  • Education and Outlook.
  • Activities that are common to most trials.
  • Linking responsibility to these activities.
  • Institutional Review Board/ Informed consent.
  • Trial- from selection to closing.
Event Details:
 
Date:                     October 10, 2012
Time:                    10:00 AM-11:10 AM PDT
Cost:                      $199 per attendee per computer terminal
Registration:         SIgn-Up on-line now.  Add to your shopping cart.
 
 
Organized by: ComplianceOnline
Invited Speakers: Madhavi Diwanji, MBA, CCRC is the President of MD Clinical Monitor. She has tremendous experience in the healthcare industry in various roles for the past 20 years. She is well rounded in all aspects of clinical trial as she has been instrumental in healthcare research with a primary focus on cardiology and oncology.
 
Deadline for Abstracts: 2012-10-10
 
Registration: http://www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=701887?channel=hummolgen
E-mail: referral@complianceonline.com
 
   
 
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