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 […]

Clinical Skills Training for Research Staff: EKG, Vital Signs, and Phlebotomy

STRATUS Center for Medical Simulation 10 Vining St, Boston, MA, United States

The Brigham Research Education Program, BWH Center for Clinical Investigation, and BWH STRATUS Center for Medical Simulation offer a clinical skills course for BWH clinical research coordinators, assistants, and study staff. This training is for research staff who need to perform EKGs, obtain vitals, and/or draw blood (phlebotomy) as part of their current job requirements at […]

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: 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 […]

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 […]

Research Connection LIVE

Hybrid

These monthly seminars are open to the community and focus on resources for the research community. They also provide an opportunity to meet and ask questions of BWH decision makers.

RCR Rounds 2023: The Peer Review Process for Manuscripts

Zoom (click website to register/receive link)

Join Karen Costenbader, MD, MPH - Faculty Director, Brigham Office for Research Careers - to learn about the peer review process for manuscripts. 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; and 3) at […]

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: Writing a Clinical Research Protocol

Zoom (click website to register/receive link)

Summary: This course is 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 Guidelines, federal and state regulations, and institutional research policies. Although many research teams require this comprehensive course as part of onboarding, […]

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, […]