MGB HRA Education: Writing a Clinical Research Protocol

Zoom (click website to register/receive link)

REGISTER via HealthStream   Summary: This MGB Human Research Affairs (HRA) course is intended for investigators and all members of the study staff involved in writing a clinical research protocol. Course content is based on the ethical conduct of human research, Good Clinical Practice (GCP) Guidelines, federal and state regulations, and institutional research policies.   […]

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 […]

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, […]

REDCap: Clinical Data Pull (CDP) Functionality

Zoom (click website to register/receive link)

REDCap can communicate with any EHR (electronic health record system) that has implemented 'SMART on FHIR' web services that allow for interoperability and limited data extraction from the EHR. In this way, REDCap can be embedded inside and launched within EPIC. This allows REDCap users to easily add patients to their projects and/or to access […]

MGB HRA Education: Informed Consent of Research Subjects (Including eConsent)

Zoom (click website to register/receive link)

CLICK HERE TO REGISTER via HealthStream   Summary: This MGB Human Research Affairs (HRA) course is for investigators and all members of the study staff. Course content is based on Good Clinical Practice (GCP), federal and state research regulations, and institutional research policies. Although many research teams require this comprehensive informed consent course as part […]

RCR Rounds 2024: Managing and 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 unanticipated problems, including adverse events, to the MGB IRB. This course is an RCR-eligible lecture and fulfills one hour toward part 2 of the NIH/NSF RCR Requirement: 1) a 4-hour MGB RCR Seminar; and 2) at least 4 […]

Brigham Research Project Manager Forum

Zoom (click website to register/receive link)

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 new skills in an informal setting.   Some meetings will be focused on a certain topic, while others will be completely devoted to open discussion. Regardless, at […]

MGB HRA Education: Sponsor-Investigator Responsibilities (IND/IDE/NSR)

Zoom (click website to register/receive link)

CLICK HERE TO REGISTER via HealthStream   Summary: This MGB Human Research Affairs (HRA) course is for MGB investigators who hold an IND, IDE, or use a NSR in an investigator-initiated clinical trial. Study staff assisting sponsor-investigators in the conduct of the clinical trial are also encouraged to attend. Course content is based on the […]

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 […]

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, […]