This webinar introduces the role of sponsor-investigator in a clinical trial and discusses regulatory and study management responsibilities. It also provides practical guidance regarding protocol design (including considerations for study monitoring and data management) and study conduct (including supervision and complying with reporting requirements). It reviews important considerations for clinical trials of drugs and devices. Further, the presenter explores how a sponsor-investigator may collaborate with internal organizational research staff and leverage external resources.
Release Date: October 7, 2021
Language Availability: English
Suggested Audiences: Clinical Research Coordinators (CRCs), Institutional Officials, Principal Investigators, Research Staff, University Faculty & Post Docs
Organizational Subscription Price: $300 per year/per site or included as part of an annual subscription to our All Access Webinar Package
Independent Learner Price: $49 per person