Clinical Compliance 2011 - Fundamentals of Clinical Research - Key players and roles for a successful and compliant research team

This training on a compliant clinical research team will focus on how Clinical Research Coordinators should work in a research team to ensure success of the clinical trial at your site.

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.

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.

- Activities that are common to most trials.

- Linking responsibility to these activities.

- Institutional Review Board/ Informed consent.

- Trial- from selection to closing.

NOTE : Use this Promocode (128600) to avail 10% discount, valid upto 4th December 2011.