Research, Discovery & Innovation

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MGB HRA Education: Human Subjects Research Recordkeeping and Record Retention

Zoom (click website to register/receive link)

Summary: This course is for investigators and all members of the study staff. It covers essential information regarding recordkeeping, documentation, and record retention requirements. Course content is based on the ethical conduct of human research, Good Clinical Practice Guidelines, federal and state research regulations, and institutional research policies. Although many research teams require this comprehensive […]

Event Series Brigham Research Project Manager Forum

Brigham Research Project Manager Forum

Zoom (click website to register/receive link)

**These sessions will be held virtually on Zoom. The link will be sent to those who register with a BWH/MGB-affiliated email address 1-2 days prior to the session**   This monthly forum is intended to build a community of peers among Research Project Managers at the Brigham by providing a space to share best practices and learn […]

MGB HRA Education: Informed Consent (Including eConsent)

Zoom (click website to register/receive link)

Summary: This course is for investigators and all members of the study staff. Course content is based on Good Clinical Practice Guidelines, federal and state research regulations, and institutional research policies. Although many research teams require this comprehensive informed consent course as part of onboarding, it is also a great refresher for experienced members of […]

RCR Rounds 2023: Managing & Reporting Unanticipated Problems Including Adverse Events

Zoom (click website to register/receive link)

Join Prapti Bisht, MBA, CIP - Director, MGB IRB Operations - to learn to manage and report unanticiapted problems, including adverse events, to the MGB IRB. This course is an RCR-eligible lecture and fulfills one hour toward part 3 of the NIH/NSF RCR Requirement: 1) CITI Online RCR Training; 2) a 4-hour MGB RCR Seminar; […]

MGB HRA Education: Study Team Data Management and Internal Quality Assurance Plans

Zoom (click website to register/receive link)

Summary: This course is for investigators and all members of the study staff. It covers essential information regarding study team data management and internal quality assurance plans. Course content is based on the ethical conduct and oversight of human research, Good Clinical Practice Guidelines, federal and state research regulations, and institutional research policies. Although many […]

MGB HRA Education: ClinicalTrials.gov Registration & Results Reporting

Zoom (click website to register/receive link)

Summary: The Clinical Trials Registration and Results Reporting course is for investigators responsible for clinical trials.gov registration and results reporting for applicable clinical trials. The course will help investigators understand the Federal and Institutional requirements for clinical trials registration and results reporting. This is a great course to include as a part of onboarding, and […]

MGB HRA Education: Clinical Research Bootcamp

Zoom (click website to register/receive link)

Summary: The Clinical Research Boot Camp course is a “clinical research 101” for investigators and all members of the study staff. Course content is based on Good Clinical Practice Guidelines, federal and state research regulations, and institutional research policies. Although many research teams require this comprehensive course as part of onboarding, it is also a […]

Biobank Portal Training

Zoom (click website to register/receive link)

The MGB Biobank Portal is a tool that links consented subjects from the MGB Biobank with their health care data from the electronic medical record (EMR) and allows researchers to request clinical samples for these subjects. This course will provide an introduction to the use of the Biobank Portal application for clinical research, including the […]

MGB HRA Education: Good Clinical Practice (GCP)

Zoom (click website to register/receive link)

Summary: This Good Clinical Practice Webinar course was developed based on the original content of the International Council of Harmonization's Guidance for Good Clinical Practice (GCP) ICH GCP E6R2, current step 4 version dated 9 November 2016. It is intended to provide researchers with training that applies GCP principles to all types of research. GCP […]

Introduction to the Research Patient Data Registry (RPDR)

Zoom (click website to register/receive link)

The Research Patient Data Registry (RPDR) brings clinical information to the researcher's fingertips and ensures the security of patient information by controlling and auditing the distribution of patient data within the guidelines of the IRB. This course will provide an introduction to the use of the RPDR (Research Patient Data Registry) application for clinical research, […]

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