WORKFORCE TRAINING
Help diversify the Clinical Research workforce one new teammate at a time.
Upskill Staff Faster, Train Thoroughly, Delegate Sooner!
The Clinical Research Fastrack Workforce Training Program is a highly intensive, accelerated, 4-day workshop course, designed to prepare your organization’s staff for the field of Clinical Research. This immersive training offers foundational instruction in ICH GCP, FDA regulations, the Informed Consent process, recruitment and retention, protocol execution, good documentation practices, and every other core competency of clinical trial facilitation. Courses are taught by active directors, managers, CRAs, and specialists from leading Clinical Research institutions across the U.S.
Clinical Research Fastrack is a trusted education provider for hundreds of the top research organizations, including Phoenix Children’s Hospital, Meridian Clinical Research, Winship Cancer Center of Emory University, Yale University, Arizona Research Center, Elligo Health Research, Ascension, MACRO Trials, and more.
Why Choose Clinical Research Fastrack?
THE VALUE OF OUR RESEARCH EDUCATION
Training new clinical research professionals can be both time-consuming and costly. By trusting us with your organization’s staff training, you can ensure that your team is practicing the hands-on skills they need for the job all while earning a GCP certification. This means that you can train faster and delegate sooner.
Program Overview
CURRICULUM BREAKDOWN:
- 4-Day Interactive Online Classroom Training (Currently held via Zoom video conferencing)
- Additional Course Materials and Online Learning
TOPICS INCLUDE
- ICH GCP Guidelines & Protecting the Rights of the Patient
- FDA Regulations
- Regulatory Affairs
- Dissection of a Protocol
- Good Documentation Practices
- Industry Language & Clinical Research Terminology
- Adverse Events & Protocol Deviations
- Recruitment & Retention of Clinical Research Subjects
- Investigator Responsibilities
- Monitoring, Quality Assurance, & Inspections
- Data Management Systems
- Clinical Trial Operations
- The Informed Consent Process
- Research Skills & Research Communications Training
Interested in onboarding your staff faster and more efficiently than ever before?
Connect with one of our
admissions team members to
apply for an upcoming course.
Clinical Research Fastrack’s curriculum meets the Minimum Criteria for ICH GCP Investigator Site Personnel Training identified by TransCelerate BioPharma as necessary to enable mutual recognition of GCP training among trial sponsors. Eligible graduates in good academic and financial standing will receive a GCP (Good Clinical Practice) Certificate (valid for 3 years) upon completion of the course.