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Clinical Research Coordinator

The CRC Training Course

Florida Medical College is open doors to a new beginning enhancing your professional health care title with the Clinical Research Coordinator. This course prepares participants to work in a Clinical Site conducting clinical trials as a Clinical Research Coordinator, assisting in the management of the study and conducting clinical investigations under the supervision of a designated Principal Investigator. This course is suitable for International Medical Graduate (IMGs), Medical Assistant, Nursing and other foreign healthcare professional that include physicians, ARNP, Register Nurse and other health-care related professionals. Applicant without previous knowledge on medical care may participate after obtain the certification on EKG and Phlebotomy that is a requirement for this course.

Clinical Research Coordinator knowledge will help Medical Assistant to initiate a new future in scientific research and you will be able to work on research places or Clinical Site as part of qualified professionals team to accomplish significant discoveries. The Clinical Research Coordinator (CRC) course is prepared based on demand of clinical sites and the SOCRA & ACCP the accredited society of Investigation in Clinical Trial. The CRC course prepares the Medical Assistant to find work in Clinical Sites as a CRC Medical Assistant and also allows the student to apply the SOCRA exam when it meets the appropriate requirements for a Certified Clinical Research Coordinator. International Medical Graduate can apply for this course, although some documents are required.

Upon completion this course the attendance should be able to:

. – Discuss the basic requirements necessary to meet the demands of a CRC in clinical practice.

. – Discuss the basic components of compliance – Law, regulation, guidance, policy and procedure.

. – Classify researches and enunciate the phases of Clinical Trials.

. – Describe components of Site Research.

. – Explain the drug/biologic development process.

. – Outline concepts for Good Clinical Practice (GCP).

. – Describe the device development process.

. – Explain the elements of Informed Consent. 

. – Describe the membership and reporting requirements of IRBs. 

. – Explain rules relating to financial disclosure. 

. – Discuss the basics of study design. 

. – Explain the rules and reporting requirements for adverse events and serious adverse events .

Course Content

  • Definition of Clinical Research Professional:
  • Good Clinical Practice.
  • FDA: Federal Regulations, codes, forms and information.
  • Research Organizations type.
  • Protection of Human Subjects.
  • Clinical Safety Data Management
Certificate of Completion Requirements:
  • Attendance: Students are expected to log in, at least, 20 hours per week.
  • Phlebotomy skills and knowledge to perform diagnostic tests of the EKG study are requirements to receive the Certificate of Completion from Florida Medical College.
  • One mandatory final exam on computer system with a passing grade will be required to pass this course. Other evaluations will be taken during course.

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