Demonstrative Documents in Clinical Research Compliance

Clinical Research Courses

Program Information:

A study’s protocol must be followed in order to maintain compliance. In order to demonstrate compliance, the study team should implement dynamic documentation that clearly and concisely tells a subject’s story of participation in the clinical study. By prioritizing adherence to the protocol and documentation of the subject’s experience, the study team will successfully demonstrate compliance and mitigate risk.

This is a 35 minute internet media player video of a voice over slide show.

A quiz concluding the presentation will summarize the topic and evaluate your understanding of the material.

Learning Objectives:

At the completion of the webinar, participants should be able to:

  • Discuss document creation and maintenance to support procedures described in the IRB-approved protocol.

Speaker:

Amber Ashley Parker, BA, CCRP

Amber is currently a Research Quality Assurance Monitor in the Office of Research Compliance (ORC) at the Children’s Hospital of Philadelphia (CHOP). Amber has over a decade of experience in the business and conduct of clinical research as a public relations representative, clinical research coordinator, research associate, and investigator. Her education and professional experience allows her to successfully consult with study teams and various organizations on research initiatives. Amber is currently pursuing a Master’s of Bioethics at the Perelman School of Medicine at the University of Pennsylvania and holds a Bachelors of Arts in Health & Societies, with a concentration in Bioethics & Society from University of Pennsylvania. She also completed a University minor in Health Care Management and Biological Basis of Behavior from the Wharton School of Business and the College of Arts & Sciences at the University of Pennsylvania. Amber is a Certified Clinical Research Professional, by the Society of Clinical Research Associates (SOCRA), and is also an active member of the Regulatory Affairs Professional Society (RAPS).

Cost:

Members – Free

Non-Members – $75.00 (includes 1 year membership)

Register:

If you are not a current member, you will be asked to create an account to view the online training.

Continuing Education Credit Hours:

SOCRA designates this educational activity for a maximum of 0.75 Continuing Education Credits for SOCRA CE.

Termination Date: 12/22/2026

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