Training
NIH Investigator Seminar Series
NIH Investigator Seminar Series
Showing 17 training in series
List of training in series
Protocol Registration and Results Reporting on Clinical Trials for the IRP
Presented by Kim Mitchell, Director Protocol Services
Research Enrolling Vulnerable Individuals - What Investigators Need to Know
Presented by Peg Sanders, RN, MSN, MA, CIP
Know Before You Go - International Research
Presented by Susan Vogel
Empowering Clinical Research: The Essential Role of Statistics and Collaborative Partnership
Presented by Nusrat Rabbee, PhD
FDA-Regulated Studies: What Investigators Need to Know
Presented by Rita Misra, PhD, MPH
NIH Investigators and Multi-Site Research
Presented by Jeffrey Rollins and Shirley Rojas
Quality Management in Clinical Research
Presented by Deborah Grady, MS, BSN, CCRC and Sharon Flynn, MS, ANP-BC, AOCNS, CRN-BC
What Investigators Need to Know About Reporting Research Related Events
Presented by Peg Sanders, RN, MSN, MA, CIP
Documentation and Document Management in Clinical Research
Presented by Elizabeth Ness, BSN, MS, RN, CRN-BC
Privacy and Confidentiality Requirements in Human Subjects Research - The Common Rule and Beyond
Presented by Heather Bridge