Ended: Oct. 23, 2018
Meghan Feldpausch, NP, Metabolism Unit
Study coordinators are responsible for collecting data at each study visit. This session offers helpful hints for creating case report forms that are clear, concise and ensure that everything is being done as it should to protect study integrity.
The goal of this session is to become familiar with the schedule of events in a protocol and learn how to translate that into creating CRFs for each study visit
Audience: Study staff new to clinical research with less than 1 year of research-related experience or experienced study staff looking to learn the basics of a new skill.
Programs: Clinical Research Skills: Intermediate Clinical Research Discussion Group: Learn Something New! Experienced Clinical Research Coordinator Beginner Clinical Research Coordinator
Categories: Clinical Research Skills Training
Sponsor: MGH Division of Clinical Research
Sessions
Oct. 23, 2018
10/23/18 12PM-1PM |
12 PM – 1 PM |
Garrod/Mendel, Floor 2, Simches Research Center
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Other Offerings
Past Offerings | |
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Learn Something New! Creating Case Report Forms to Help Study Visits Run Smoothly and per Protocol |
Sept. 29, 2020
09/29/20 |
Learn Something New! Creating Case Report Forms to Help Study Visits Run Smoothly and per Protocol |
Oct. 1, 2019
10/1/19 |