Research Training & Development
You Need to Reach the Finish Line.
Like Anything Else, that Takes Training.
Your study may be short staffed. It may be operating on a tight budget. Yet one thing it cannot afford to be is derailed due to lack of experience or knowledge.
Quality research training is in demand because the increasing needs of clinical research demand it.
IMARC offers affordable training and development programs that will get your clinical research staff – coordinators, investigators, monitors, project managers and others – up to speed fast.
Download Research Training & Development Sales Sheet
Be trained to:
- Implement the framework required to stay compliant.
- Navigate the regulatory maze with GCP training tailored specifically to your study team.
- Run your own investigator-initiated IDE or IND study with existing staff.
- Manage specific phases or processes while staying focused on achieving approval.
Expert Clinical Research Training for:
- Monitors
- Research Coordinators
- Investigators
- Project Managers
Training Sessions
Expand your regulatory knowledge of study operations with these courses:
- Introduction to Research Coordinating
- Monitoring "Musts"
- Understanding Clinical Research Sites (for Project Managers and Monitors)
- Clinical Site Management
- Human Subject Protection
- Monitoring Device Studies
- Device vs. Drugs
- Monitoring Team Roles for Global Studies
- Warning Letters… and the Implications for You
Training Techniques
IMARC training solutions are designed to provide you with a better understanding of your specific research setting and how it functions. These informative, interactive and inspirational solutions include:
- Didactic Presentations
- Group Activities
- Case Study Discussions
- Warning Letter Reviews & Discussions
- Games & Quizzes
- Virtual Study Experiences
For additional information on IMARC Research’s training and development program, please contact John E. Lehmann at 440.801.1540.