Roles and Responsibilities of a New Clinical Monitor Assistant (CMA)

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.

This session is an important tool in preparing a CMA to be better organized. This training will outline all the tasks and responsibilities of a CMA, how to get started, how to be able to maintain a healthy and productive collaboration with the CRCs, suggest tips for helping you meet the deadlines and help you solve any issues and/or problems of any kind that may come up on the way.

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.