Fourth Annual Clinical Research Symposium
The role of clinical research coordination is extremely vast and varies greatly from clinical trial to clinical trial. However, common threads such as the Common Rule, ICH and GCP guidelines are ever-present in the clinical research community. Continuing education on various topics is essential for successful trial coordination. Clinical research is an ever-evolving career, where a research coordinator is often asked to wear many hats from trial to trial and keep current on current regulations, guidelines, and best practices. Education is essential. Increased education will hopefully lead to increased patient safety and improved data quality for each clinical trial.
The Medical College of Wisconsin designates this activity for up to 4 hours of participation for continuing education for allied health professionals.
Target Audience
Medical Students
Learning Objectives
At the conclusion of this activity, I will be able to:
- Identify methods to successfully work with patients an families with low health literacy
- Recognize potential barriers to clinical trial minority accrual
- Possess methods for overcomming barriers to clinical trial minortiy recruitment and retention
- Understand the ethical considerations involving underserved populations and clinical trial accrual
Activity Director:
James Thomas, MD
Rebecca Selle
Melinda Stolley, PhD
Ryan Spellacy, PhD
All persons in control of content have NO relevant financial relationships to disclose with the exception of the following and in accordance with the ACCME® standards for Commercial Support Number 6, these relationships were reviewed via the MCW conflict of interest resolution process and resolved.
Available Credit
- 4.00 AMA PRA Category 1 Credit(s)™AMA PRA Category 1 Credit(s)™
- 4.00 Hours of ParticipationHours of Participation credit.

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