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. |
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