The Clinical Trials Guru
Portal About Me Get In The Industry Intro To Clinical Research Start A Site Consulting Podcast
PortalAbout MeGet In The IndustryIntro To Clinical ResearchStart A SiteConsultingPodcast
The Clinical Trials Guru
Clinical Trials In Plain English

Documenting Adverse Events For Clinical Research Coordinators

One of the more important teaching points in our CRC Academy is adverse event reporting for clinical research coordinators. In this video I share some tips for clinical trial coordinators who are tasked with proper reporting documentation and processing.

Dan SferaJune 30, 2021Comment
Facebook0 Twitter LinkedIn0 Reddit Tumblr 0 Likes
Previous

Do Not Ever Lie To Get A Clinical Research Job! EVER!!!

Dan SferaJuly 1, 2021
Next

The Hurdles A Clinical Research Tech Vendor Needs To Jump Through To Land Sponsor Contracts

Dan SferaJune 28, 2021

Join Over 10,000+ Subscribers Getting Exclusive Content, Private Q&A's, Giveaways and More!

Thank you!

CRA Academy | CRC Academy | My Consulting Firm/Work With Me | Get My Book! | Archives/YouTube Channel

This site is managed by Sfera Media and DSCS Sweat Equity & Investments, LLC

All rights reserved.