Margaret Rankovic, MEd, CIP
Margaret Rankovic is an Associate Director for Content and Education and a member of the Program Advisory Committee. She is the program manager and lead developer for educational content for human subjects research, IRB administration, clinical research coordinator, principal investigator, information security, and good clinical practice (GCP) courses. Ms. Rankovic is also a certified IRB professional with extensive knowledge of federal regulations, including FDA and HHS. She received her BA and MEd in research, statistics, and evaluation from the University of Virginia.
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GCP for Clinical Investigations of Drugs and Devices (FDA)
Ideal for individuals proposing to conduct clinical trials of drugs, biologics, and devices primarily in the U.S.
Revised Common Rule: Overview of Revisions
It has been more than six months since the revised Common Rule’s implementation date, revisit the revisions it made using thi...
Revised Common Rule: Revisions to Definitions
In-depth review of revisions to the definitions section of the Common Rule. Covers new terms added, updates to existing definit...
Revised Common Rule: Revisions to Informed Consent
Explores the revised Common Rule’s updates to informed consent. Focuses on key changes, new elements, and updates to existing...
Participating in Vaccine Research (Free Webinar)
Learn about what to expect when participating in vaccine research.
IRB – Biomedical Focus
Provides foundational training for IRB members involved in the review of biomedical human subjects research.
IRB – Biomedical and Social-Behavioral-Educational Combined
Provides foundational training for IRB members involved in the review of both biomedical and social-behavioral-educational huma...