A Beginner’s Guide to Being a Sponsor-Investigator

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

Questions? Contact Us
Scroll Down Arrow

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.

Webinar Demo:

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: Included as part of an 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

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

Learning Objectives:

  • 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)

Learn More

Your Name(Required)
I'd Like To Receive Emails From CITI Program
This field is for validation purposes and should be left unchanged.