Make It Short!
(Acronyms & Abbreviations)
Who am I?
(Roles & Responsibilities)
What Am I Doing?
(Tasks)
Doing It Right
(Ethics and Compliance)
Today is the Day!
(Clinical Trials Day)
100

AI/ML

What is Artificial Intelligence/Machine Learning?

100

Research professional who ensures research adheres to all regulations, guidelines, and upkeeps the appropriate research documents

Who is a Clinical Research Regulatory Specialist/ Coordinator?

100

Comprehensive, detailed plan or "living document" that outlines the entire rationale, design, methodology, and ethical considerations of a research study.

What is a research protocol?

100

The signed and dated document that allows a covered entity to use and/or disclose PHI for research purposes.

What is HIPAA Authorization?

100

The date of Clinical Trials Day

What is May 20?

200

ERDs

What is Ethical and Religious Directives for Catholic Health Care Services?

200

Research professional who manages the day-to-day activities of a clinical trial

Who is a Clinical Research Coordinator?

200

The process that ensures a participant receives and sufficiently comprehends information in order to decide and communicate voluntary participation in research

What is the informed consent process?

200

The entity responsible for review and approval of protocols to ensure ethical conduct of human subject research.

What is the Institutional Review Board (IRB)?

200

James Lind

Who is often considered to be the first person to conduct a randomized clinical trial?
300

CA

What is a Coverage Analysis?

300

Research professional who develops new medications and/or prepares, compounds, dispenses research medications

Who is a Research/Investigative Drug Pharmacist?

300

Often called "bench-to-bedside," this type of research accelerates the transformation of basic scientific discoveries into practical, clinical applications—such as diagnostics, therapeutics, and medical procedures—to improve human health

What is translational research?

300

The appropriate documentation that establishes the regulatory review relationship between a research site institution and a single/central IRB

What is a reliance agreement OR IRB Authorization Agreement?

300

The disease that was investigated during the first randomized clinical trial

What is scurvy?

400

REDCap

What is Research Electronic Data Capture?

400

Research professional who designs, analyzes, and interprets data from clinical research studies, contributing to advancements in patient care and treatment

Who is a Biostatistician?

400

A framework for establishing and maintaining data integrity comprising the qualities of Attributable, Legible, Contemporaneous, Original, Accurate, Complete, Consistent, Enduring, and Available

What is ALCOA+?


400

The term for OSF process of institutional review and authorization to conduct clinical trials in conjunction with appropriate IRB review/approval.

What is Research Administration/Institutional Permission?

400

True or False: Clinical Trials Day is an international commemoration

What is true?

500

SUSAR

What is Suspected Unexpected Serious Adverse Reaction?

500

An individual who both initiates and conducts an investigation and under whose immediate direction the investigational drug is administered or dispensed.


Who is a Sponsor-Investigator?

500

Department providing a service that is necessary to conduct a clinical trial protocol: Pharmacy, for example

What is an ancillary department?

500

When personal financial or institutional interests potentially or actually interfere with the primary interests of research integrity and participant well-being.

What is a conflict of interest?

500

To recognize the impact of clinical research on medical progress, celebrate clinical research professionals, and thank participants for their contribution to developing new, safe, and effective treatments

What is the purpose of International Clinical Trials Day?

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