The Ophthalmic Clinical Research Coordinator

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Elements of Clinical Research

https://saatlasacuitypublic.blob.core.windows.net/videos/Mod%2001%20-%20Clinical%20Research%20Coordinator.mp4; Mod 1 - Clinical Research Coordinator; 14:31 https://saatlasacuitypublic.blob.core.windows.net/videos/Mod%2002%20-%20Clinical%20Trial%20Lifecycle.mp4; Mod 2 - Clinical Trial Lifecycle; 4:13 https://saatlasacuitypublic.blob.core.windows.net/videos/Mod%2003%20-%20Pre%20Clinical%20Research.mp4; Mod 3 - Pre Clinical Research; 9:09 https://saatlasacuitypublic.blob.core.windows.net/videos/Mod%2004%20-%20Types%20of%20Research.mp4; Mod 4 - Types of Research; 9:48; https://saatlasacuitypublic.blob.core.windows.net/videos/Mod%2005%20-%20Ethical%20Principles%20in%20Human%20Research.mp4; Mod 5 - Ethical Principles in Human Research; 14:54; https://saatlasacuitypublic.blob.core.windows.net/videos/Mod%2006%20-%20How%20It%20Is%20Regulated.mp4; Mod 6 - How It Is Regulated; 16:24; https://saatlasacuitypublic.blob.core.windows.net/videos/Mod%2007%20-%20How%20Clinical%20Trials%20Are%20Initiated.mp4; Mod 7 - How Clinical Trials Are Initiated; 21:33; https://saatlasacuitypublic.blob.core.windows.net/videos/Mod%2008%20-%20How%20Clinical%20Trials%20Are%20Conducted.mp4; Mod 8 - How Clinical Trials Are Conducted; 13:24; https://saatlasacuitypublic.blob.core.windows.net/videos/Mod%2009%20-%20Data,%20Electronic%20Case%20Report%20Form,%20Source.mp4; Mod 9 - Data, Electronic Case Report Form, Source; 14:20; https://saatlasacuitypublic.blob.core.windows.net/videos/Mod%2010%20-%20Documentation,%20ALCOA,%20Monitoring.mp4; Mod 10 - Documentation, ALCOA, Monitoring; 10:08; Mod 10 - Documentation, ALCOA, Monitoring; 10:08;

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Reference Section

Natural History
https://www.fda.gov/regulatory-information/search-fda-guidance-documents/rare-diseases-natural-history-studies-drug-development

Real World Evidence
https://www.fda.gov/science-research/science-and-research-special-topics/real-world-evidence

Nuremberg Code
["Trials of War Criminals before the Nuremberg Military Tribunals under Control Council Law No. 10", Vol. 2, pp. 181-182. Washington, D.C.: U.S. Government Printing Office, 1949.]

Belmont Report
https://www.hhs.gov/ohrp/sites/default/files/the-belmont-report-508c_FINAL.pdf

Declaration of Helsinki
https://www.wma.net/what-we-do/medical-ethics/declaration-of-helsinki/doh-oct2008/

International Conference on Harmonization Good Clinical Practice (ICH GCP)
https://database.ich.org/sites/default/files/E6_R2_Addendum.pdf

Code of Federal Regulations for Clinical Trials
https://www.fda.gov/science-research/clinical-trials-and-human-subject-protection/regulations-good-clinical-practice-and-clinical-trials

CITI Program
https://about.citiprogram.org/series/good-clinical-practice-gcp/

Institutional Biosafety Committee Guidance Document
https://osp.od.nih.gov/wp-content/uploads/NIH_Guidelines.pdf

Endpoints
https://toolkit.ncats.nih.gov/glossary/endpoint/

© 2025 Atlas Acuity, LLC
contact@atlasacuity.com

© 2025 Atlas Acuity, LLC
contact@atlasacuity.com