This course provides a tactical approach to clinical protocol development and implementation. The course includes evidence-based strategies, best practices from field experts, and standard tools to aid the protocol authoring process. A well-thought-out and well-written protocol ensures high-quality science and strengthens the quality of the endpoints. With an effective protocol, investigators can accelerate development and study completion, ensure regulatory and data compliance, and avoid unnecessary financial drain.
This course was developed by Therica Miller and co-authored by Michelle Mack, Jennifer Hofecker-Burgess, Heather Chen, and Carrie Thomas. The course was peer reviewed by experts.
Language Availability: English
Suggested Audiences: Advanced Research Coordinators, Clinical Investigators, Faculty, Program Managers, Project Managers, Project Scientists, Recently awarded grant recipients with concepts in the clinical trial setting, Research teams charged with assisting researchers with proposal execution, Sponsor-Investigators, Students
Organizational Subscription Price: $675 per year/per site for government and non-profit organizations; $750 per year/per site for for-profit organizations
Independent Learner Price: $99 per person