DCR-RCR Series: QI Bootcamp for Clinical Researchers and Study Staff

QI Bootcamp for Clinical Researchers and Study Staff The QI Program and the MGH Division of Clinical Research are excited to offer QI Bootcamp. QI Bootcamp is a “clinical research 101” for study staff and investigators. The goal of the course is to review GCP guidelines and institutional policies, and instruct study staff and investigators...

Good Clinical Practice in Research at an Academic Research Institution

November 14 | November 21 | December 5 | December 12 Sponsored by the MGH Division of Clinical Research, Partners Human Research Committee and Partners Human Subjects Quality Improvement Program Good clinical practice (GCP) is an international ethical and scientific quality standard for designing, conducting, recording and reporting human subjects’ research. GCP guidelines define the...

Good Clinical Practice in Research at an Academic Research Institution

November 14 | November 21 | December 5 | December 12 Sponsored by the MGH Division of Clinical Research, Partners Human Research Committee and Partners Human Subjects Quality Improvement Program Good clinical practice (GCP) is an international ethical and scientific quality standard for designing, conducting, recording and reporting human subjects’ research. GCP guidelines define the...

Good Clinical Practice in Research at an Academic Research Institution

November 14 | November 21 | December 5 | December 12 Sponsored by the MGH Division of Clinical Research, Partners Human Research Committee and Partners Human Subjects Quality Improvement Program Good clinical practice (GCP) is an international ethical and scientific quality standard for designing, conducting, recording and reporting human subjects’ research. GCP guidelines define the...

Good Clinical Practice in Research at an Academic Research Institution

November 14 | November 21 | December 5 | December 12 Sponsored by the MGH Division of Clinical Research, Partners Human Research Committee and Partners Human Subjects Quality Improvement Program Good clinical practice (GCP) is an international ethical and scientific quality standard for designing, conducting, recording and reporting human subjects’ research. GCP guidelines define the...

Data Management and Research Integrity

This final Responsible Conduct of Research (RCR) session of the 2018-2019 academic year will discuss: management of research data for publication and sharing and research integrity in collaborations and publications. Speakers: Gretchen Brodnicki, JD, Dean for Faculty and Research Integrity, HMS Jessica Haberer, MD, MS, Associate Professor of Medicine, HMS; Director of Research, MGH Center...

Rigor and Reproducibility in Scientific Research

Rigor and reproducbility are key factors in strong scientific research. This seminar will discuss the consideration of these factors in research design, and how to describe them in NIH funding applications, including: Rigor of prior research (scientific premise) Experimental design for robust, unbiased results Consideration of relevant biological variables Authentication of key biological and/or chemical...

Mock NIH Study Section

Would you like to know what happens after you send your grant application to NIH? This “mock” study section will provide a window into the NIH grant review process. The session will also feature HMS faculty with extensive NIH study section experience. Speakers: Dennis Brown, PhD, Professor of Medicine, HMS; Director, Office for Research Career...

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