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REDCap: Getting Started

Zoom (click website to register/receive link)

Summary: In collaboration with the Harvard Catalyst, REDCap is a free, secure, web-based application hosted by MGB Research Computing and designed to support electronic data capture for research studies. To learn more about REDCap visit: http://rc.partners.org/edcredcap. This course will provide a high level overview of the REDCap tool. Learn about study start up, project life cycles, data […]

RCR Rounds 2024: IRB 101: Collaboration, Partnership, and Research Ethics

Zoom (click website to register/receive link)

Join Benjamin Silverman, MD - Senior Chair of the MGB IRB - to learn about working with 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 hours of RCR-eligible lectures. Please register.

MGB HRA Education: Clinical Research Bootcamp

Zoom (click website to register/receive link)

CLICK HERE TO REGISTER via HealthStream   Summary: This MGB Human Research Affairs (HRA) course is a comprehensive human subjects research training course for investigators and all members of the study staff. Course content is based on the ethical principles of human research protections, Good Clinical Practice (GCP) Guidelines, federal and state research regulations, institutional […]

MGB HRA Education: ClinicalTrials.gov (CT.gov) Registration & Results Reporting

Zoom (click website to register/receive link)

REGISTER via HealthStream   Summary: This MGB Human Research Affairs (HRA) course is strongly recommended for investigators responsible for ClinicalTrials.gov registration and results reporting for applicable clinical trials. This course is also recommended for members of the study staff assisting the investigator with entering information in records, maintaining records, and reporting results. The course will […]

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: eConsent Functionality

Zoom (click website to register/receive link)

Mass General Brigham (MGB) has developed a REDCap eConsent Framework that will turn the paper-based informed consenting processes into an electronic informed consent process that researchers can use for Institutional Review Board (IRB) reviewed and approved studies. The MGB REDCap eConsent Framework will allow users to implement a combination of the validated components to design […]

RCR Rounds 2024: Academic Medicine, Industry, and Collaborative Research in the Era of Emerging Technologies and Precision Health

Zoom (click website to register/receive link)

Join Samia Mora, MD, MHS to learn about academic medicine, industry, and collaborative research in the era of emerging technologies and precision health. 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 hours of RCR-eligible […]

MGB HRA Education: Recordkeeping and Record Retention Requirements

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 and covers essential information regarding recordkeeping, documentation, and record retention requirements. Course content is based on the ethical conduct of human research, Good Clinical Practice (GCP) Guidelines, federal and state […]

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.   […]

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