Are you a New Clinical Monitor Assistant (CMA)? Your Roles and Responsibilities and Tips for Getting you Organized

This webinar will get you familiarized with the responsibilities of a CMA during a clinical trial, help you get started and well organized, help you build up a healthy and productive collaboration within a clinical trials team as well as suggest you tips for solving/avoiding problems and issues.

Why Should You Attend:

• Are you a new Clinical Monitor Assistant (CMA)?
• Not new but looking for ways to get better organized and improve your collaboration with the team?
• Are you a new Clinical Research Associate who needs all the help you can get on your trials?

Watching the demand for Clinical Research Associate (CRA) positions increasing so rapidly, it is only reasonable to expect an increase as well as in Clinical Monitor Assistants (CMAs) positions. This rapid increase in CRC positions also increases the urgent need of well prepared and suitable assistants for supporting and assisting a CRC.

Areas Covered in the Seminar:

• The role of a CMA in a Clinical Trials Team.
• Tasks and responsibilities.
• Tips for getting better organized.
• Issues to solve/avoid.
• Maintain a productive and smooth collaboration with the team.
• Setting up and maintaining trial files.
• Responsibility during audits and inspections.

Who Will Benefit:

This webinar will provide valuable assistance to:

• People interested in setting up a Clinical Trials Team for exploring the field of Clinical Research
• New Clinical Monitor Assistants
• Clinical Monitor Assistants exploring possible new ways of getting organized
• Clinical Research Coordinators
• New Project Managers

Event Details:

Date:             September 13, 2012

Time:             10:00 AM - 11:00 AM PDT

Cost:             $199 per attendee per computer terminal

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