Looking to start a career as a Clinical Research Coordinator or Regulatory Coordinator? Clinical Trial Experts has developed an intensive training program designed to meet the needs of coordinators who have less than one year of experience or who have never received formal training. It is useful to anyone who requires a fast, thorough introduction to clinical research trial conduct, Good Clinical Practice and the federal regulations governing research. The class is geared toward providing practical information to get students "up and running" in the clinic, with many tools and templates to assist with study implementation. 

Course topics include: 

Informed consent, clinical trial initiation, FDA forms and procedures, regulatory documents and binder maintenance, source documents, study initiation and close-out visits, compliance and retention, drug compliance/storage/documentation, IRB submissions and HIPAA, adverse events and safety monitoring, quality assurance audits and monitor visits and preparing for FDA audits.

Advantages:

-Individual training & preparation

-CTE will help you in create a curriculum vitae (CV), also known as a resume

-At the end of course, you will be provided with certification of completion

-Available resources after training program

-Possible internships at local research facilities