Association of Clinical Research Professionals (ACRP) – Wisconsin Chapter

This webinar will discuss the best practices in various areas of clinical research management of investigator-initiated trials (IITs) and detail how to navigate common challenges.

This live webinar will explore diversity through a global lens by tapping into the perspectives of industry leaders who will address how we can broaden access to a wide range of underrepresented groups, including those who possess attributes linked to troubling and challenging health disparities.

Come learn and discuss with us the growth and diversification of the clinical research workforce.

Join this live webinar for an informative session on some of the tools of the clinical research trade: data extraction and adverse event reporting. The presenter will review adverse events and serious adverse event reporting, medical record data extraction and collection, and review SAE-related medical...

Join this live webinar program as we delve into medical devices and investigational medical devices. The presenter will provide information on FDA regulations and ISO requirements along with the similarities and differences for device trials conducted at the research site.

This live webinar will challenge attendees to self-reflect on their own leadership practices and how those may be in need of transformation. Whether you are an aspiring leader, new supervisor, or seasoned manager in clinical research, you will come away from this webinar with valuable knowledge for your virtual leadership tool kit that will help promote transformational leadership practices for your own sake and for the benefit of your team.

Clinical trial professionals with an interest or role in the onboarding and education of new staff are encouraged to attend this live webinar and learn valuable best practices from the steps taken, barriers encountered, and resources available during one clinical trial site’s journey toward realizing its goal for optimal efficiency.

This live webinar will address practical ways that stakeholders in research can help improve the creation of ICFs and better the overall process to ensure patients have a fuller understanding of the risks, commitment, and cost of agreeing to participate in a clinical trial.

Current efforts to improve diversity in clinical research fall short for the LGTBQIA+ population.