Team Member Margaret Rankovic

Margaret Rankovic, MEd

CITI Program

Margaret Rankovic is the 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 also previously held her certified IRB professional credential for 9 years and has 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.

Browse This Author's Contributions

GCP for Clinical Investigations of Drugs and Devices (FDA) GCP for Clinical Investigations of Drugs and Devices (FDA)
CME/CEU
Series: Good Clinical Practice (GCP)

Ideal for individuals proposing to conduct clinical trials of drugs, biologics, and devices primarily in the U.S.

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Revised Common Rule: Overview of Revisions Revised Common Rule: Overview of Revisions
Featured
Series: Webinars

It has been more than six months since the revised Common Rule’s implementation date, revisit the revisions it made using thi...

calendar showing common rule compliance date
Revised Common Rule: Revisions to Definitions Revised Common Rule: Revisions to Definitions
Featured
Series: Webinars

In-depth review of revisions to the definitions section of the Common Rule. Covers new terms added, updates to existing definit...

one following another meaning revision
Revised Common Rule: Revisions to Informed Consent Revised Common Rule: Revisions to Informed Consent
Featured
Series: Webinars

Explores the revised Common Rule’s updates to informed consent. Focuses on key changes, new elements, and updates to existing...

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Participating in Vaccine Research (Free Webinar) Participating in Vaccine Research (Free Webinar)
Featured
Series: Complimentary COVID-19 Training

Learn about what to expect when participating in vaccine research.

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IRB Member – Biomedical Focus IRB Member – Biomedical Focus
CME/CEU
Series: Human Subjects Research (HSR)

Provides foundational training for IRB members involved in the review of biomedical human subjects research.

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IRB Member – Biomedical and Social-Behavioral-Educational Combined IRB Member – Biomedical and Social-Behavioral-Educational Combined
CME/CEU
Series: Human Subjects Research (HSR)

Provides foundational training for IRB members involved in the review of both biomedical and social-behavioral-educational huma...

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IRB Administrator Professional Development and Self-Advocacy IRB Administrator Professional Development and Self-Advocacy
Featured
Series: Webinars

Learn how to grow and develop yourself as an IRB administrator.

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On Research Podcast - PRIM&R 2023: Insights and Takeaways On Research Podcast - PRIM&R 2023: Insights and Takeaways
Featured

Season 1 - Episode 13
This is a special edition of On Research with CITI Program. Guest hosted by Margaret Rankovic, Director of Content and Education at CITI Program, this podcast provides a recap, insights, and key takeaways from the recently concluded PRIM&R 2023 conference.

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