Workforce Training

Outsource your staff training for more efficient onboarding.

Everything you need to train your Clinical Research staff — faster.

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, 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, Winship Cancer Center of Emory University, Yale University, Arizona Research Center, Elligo Health Research, Ascension, MACRO Trials, VirTrials, and more.


Why Choose Clinical Research Fastrack

The Value of Outsourcing

Training new clinical research professionals can be both time-consuming and costly. By outsourcing your organization’s staff training, you can save time, maximize efficiency and avoid hiccups throughout the onboarding process.

Clinical Research Fastrack’s Clinical Research Workforce Training is a revolutionary, industry-led program designed to quickly meet the staffing needs of individual research organizations. Course instructors are active professionals from many of the leading Clinical Research organizations in the U.S., who provide years of practical knowledge and experience, condensed into an efficient 4-day workshop course.

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
  • Tying It All Together

This ICH E6 GCP Investigator Site Training 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.

This nursing continuing professional development activity was approved by the Georgia Nurses Association, an accredited approver by the American Nurses Credentialing Center’s Commission on Accreditation.