ONBOARD & UPSKILL YOUR TEAM
Clinical Research Industry Training
3-day training to refresh your teams skills for improved trial performance
Better Training. Better Trials.
Clinical Research Fastrack’s Industry Training is a high-impact workforce solution that transforms clinical research sites into hubs of operational excellence in just three days. By standardizing skills across your entire staff, our training ensures every team member operates with a unified understanding of GCP and protocol execution. This intensive workshop removes the training burden from Principal Investigators and Site Managers, delivering a “Trial-Ready” team that is equipped to handle complex trials with precision and reduced risk of costly data queries.
Investing in this 3-day course provides an immediate ROI by increasing site efficiency and making your organization more attractive to sponsors and CROs. Beyond compliance, this program fosters a culture of professional competence that improves staff retention and speeds up study start-up times. Ultimately, this will act as a strategic engine for growth, ensuring your workforce is prepared to deliver high-quality data and maintain the highest standards of industry excellence.
Training Outline:
- Phase 1: Pre-Study (8-10 Hours): Master the terminology at your own pace before we meet live.
- Phase 2: Live Technical Intensive (Days 1–3): Deep dive into FDA regulations, protocol dissection, and data management with industry experts via Zoom.
- Phase 3: Post-Study Mastery: 30 hours of self-paced curriculum to lock in your expertise.
Course Breakdown
Days 1-3:
The 3 days cover core principles of clinical research including:
- ICH Good Clinical Practice (R3)
- Protecting Patients Rights
- FDA Regulations
- Regulatory Affairs
- Dissecting a Protocol
- Adverse Event Reporting and Deviations
- Good Documentation Practices
- Data Management
- Clinical Trial Operations
- Monitoring and QA
- Recruitment and Retention
- The Informed Consent Process
Why train your staff with Fastrack?
Training with Clinical Research Fastrack provides your team with an immediate competitive edge by bridging the gap between theoretical knowledge and real-world application. Our curriculum is developed and delivered by active industry experts, ensuring your staff masters the most current regulatory standards and operational efficiencies. By choosing Fastrack, you are not just checking a compliance box; you are empowering your workforce with the practical skills and confidence needed to reduce errors, accelerate study timelines, and deliver the high-quality data that sponsors demand.
Let's customize a solution for your team!
Connect with us to explore customized training, CAPA support, or targeted team refresher sessions.
Looking to refresh your team's skills?
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.