Experienced Clinical Research Coordinator

This program targets the experienced Clinical Research Coordinator (CRC) with more than 2 years of experience, Senior Clinical Research Coordinators and Project Managers.

Individuals in this program have a fair understanding of MGH policies and procedures, are very familiar with the conduct of clinical trials, possess adequate understanding of GCP’s and are able to apply to current practice.

This program focuses on the administrative processes behind the implementation and conduct of clinical trials.

September


26

Sep

IRB Roundtable: Continuing Review and Amendments

Sponsor: MGH Division of Clinical Research   Producer: Division of Clinical Research

Sept. 26, 2019 @ 12 PM

Clinical Research Investigator Beginner Clinical Research Coordinator Experienced Clinical Research Coordinator Clinical Research Ethical Oversight IRB

October


17

Oct

IRB Roundtable: Amendments and Reporting to the IRB

Sponsor: MGH Division of Clinical Research   Producer: Division of Clinical Research

Oct. 17, 2019 @ 12 PM

Beginner Clinical Research Coordinator Clinical Research Investigator Experienced Clinical Research Coordinator Clinical Research Ethical Oversight IRB

November


14

Nov

IRB Roundtable: Consent Form Writing

Sponsor: MGH Division of Clinical Research   Producer: Division of Clinical Research

Nov. 14, 2019 @ 11 AM

Beginner Clinical Research Coordinator Clinical Research Investigator Experienced Clinical Research Coordinator Clinical Research Ethical Oversight IRB

December


12

Dec

IRB: New Submission

Sponsor: MGH Division of Clinical Research   Producer: Division of Clinical Research

Dec. 12, 2019 @ 12 PM

Beginner Clinical Research Coordinator Clinical Research Investigator Experienced Clinical Research Coordinator IRB

No Current Offerings


IRB Issues for the Bench and Desk Scientist

Sponsor: MGH Division of Clinical Research   Producer: Division of Clinical Research

Last Offered: Nov. 6, 2018

Experienced Clinical Research Coordinator Clinical Research Investigator Ethical Oversight IRB

What Does the IRB Really Want? How to Write a Human Studies Protocol

Sponsor: MGH Division of Clinical Research   Producer: Division of Clinical Research

Last Offered: Nov. 12, 2018

Experienced Clinical Research Coordinator Clinical Research Investigator Beginner Clinical Research Coordinator Ethical Oversight IRB