Vulnerability in Research 101
CHÉOS Scientist Dr. Anita Ho discusses the concept of vulnerability when it comes to participation in clinical research.
Read MoreCHÉOS Scientist Dr. Anita Ho discusses the concept of vulnerability when it comes to participation in clinical research.
Read MoreThe 18th installment in our Clinical Research 101 series is by Project Manager Allison Coleman, and discusses adverse events in clinical research, how to collect and report them, and why they're important
Read MoreCHÉOS Project Manager Shoshana Parker shares an insight into the role of clinical research coordinators in clinical trials
Read MoreLeslie Love, Senior Project Manager at CHÉOS, discusses protocol deviations, how to avoid them, and what to do when they occur
Read MoreDana Nohynek, Director of Regulatory Affairs and Quality Assurance, provides an overview of how and why to manage risk in clinical trials.
Read MoreProject Manager Laura Zunino provides an overview of the informed consent process, why it matters, and how to improve it.
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