A Beginner’s Guide to Being a Sponsor-Investigator

A primer for understanding the sponsor-investigator role and responsibilities in clinical research.

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About this Webinar


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.

Language Availability: English

Suggested Audiences: Clinical Research Coordinators, Institutional Officials, Principal Investigators, Research Staff, University Faculty & Post Docs

Organizational Subscription Price: $300 per year/per site or included as part of the $1,000 annual subscription to our All Access Webinar Package
Independent Learner Price: $49 per person


Webinar Content


A Beginner’s Guide to Being a Sponsor-Investigator New Content

Presented by: Melissa A. Scotti, PhD, CIP - Northwell Health

By the end of this webinar, you should be able to:

  • Define the sponsor-investigator role.
  • Identify sponsor-investigator regulatory responsibilities.
  • Discuss considerations for study planning including: study design, leveraging resources, and working with research/institutional support services.

Recommended Use: Required
ID (Language): 20520 (English)


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