Are you a new Clinical Research Coordinator? Tips on how to get started, what to expect 2010

This clinical research webinar will discuss the role and responsibilities of an efficient well rounded Clinical Research coordinator and what to do pre and post trial period to comply with GCP and other regulations.

Areas Covered in the Seminar:

• ICH guidelines and Good Clinical Practice (GCP).
• Types and Phases of Clinical Trials.
• 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.

Who Will Benefit:

This webinar will provide valuable assistance to all personnel in:

• Healthcare providers interested in exploring the field of Clinical Research
• New Clinical Research Coordinators (1-2 years)
• New Principal Investigators
• Administrative managers in charge of Clinical Research
• Regulatory Compliance Associates and Managers