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.

Coming Soon


MGH Division of Clinical Research

IRB Roundtable: Continuing Review and Amendments

Sponsored by the MGH Division of Clinical Research, the Partners Human Research Office (IRB) and the Partners Human Research Quality Improvement Program (QI). Speakers: Jo O'Driscoll-Davis, Assistant Director for Continuing Review and Administrative Chair Michael Ducey, Senior Human Resource Specialist …

MGH Division of Clinical Research

Good Clinical Practice in Research at an Academic Research Institution

Good Clinical Practice in Research at an Academic Research Institution May 28 | June 04 | June 11 | June 18 | June 25 185 Cambridge Street | Simches 3rd Floor, Room 3.110 Sponsored by the MGH Division of Clinical …

MGH Division of Clinical Research

IRB Roundtable: Amendments and Reporting to the IRB

Sponsored by the MGH Division of Clinical Research, the Partners Human Research Office (IRB) and the Partners Human Research Quality Improvement Program (QI). Speaker:Jo O'Driscoll-Davis, Assistant Director for Continuing Review and Administrative Chair Per Federal Regulations, and Partners HRC policies, …

MGH Division of Clinical Research

IRB Roundtable: Consent Form Writing

Did you know that most of your research subjects are reading at the 8th-grade level or lower? Learn how to write the simplest, clearest consent forms, so that every one of your subjects can be fully informed. This workshop will …

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MGH Division of Clinical Research

Ethics in Clinical Research

Ethics and Clinical Research Protocols Sponsored by the MGH Division of Clinical Research Melissa Frumin, M.D., M.S., Chair, Partners IRB In this course, participants will receive an overview of the ethical foundation of Human Subject Protection in clinical research. This …

MGH Division of Clinical Research

IRB Issues for the Bench and Desk Scientist

Sponsored by the MGH Division of Clinical Research and the Human Research Committee Elizabeth Hohmann, MD, Chair and Physician Director, Partners Human Research Committee The purpose of this seminar is to discuss ethical, regulatory, and institutional issues relevant to analysis …

MGH Division of Clinical Research

Spotlight Series: ICH E6 Guideline Revisions

Sponsored by the MGH Division of Clinical Research Daniel Jones, MSN RN Senior QA/QI Specialist of the Partners Quality Improvement Program Did you know that the E6 Guidelines were revised and adopted by ICH on 12/15/2016? Who do these revisions …

MGH Division of Clinical Research

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

Sponsored by the MGH Division of Clinical Research and the Human Research Committee Elizabeth Hohmann, M.D., Chair and Physician Director, Partners Human Research Committee This practical lecture addresses "Full Review Protocols" - those of more than minimal risk which must …