Adverse Events 101
The 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 MoreMay 4, 2021
The 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
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CHÉOS Project Manager Shoshana Parker shares an insight into the role of clinical research coordinators in clinical trials
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Leslie Love, Senior Project Manager at CHÉOS, discusses protocol deviations, how to avoid them, and what to do when they occur
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CHÉOS Scientist Dr. Anita Ho discusses the idea of vulnerability when it comes to participation in clinical research.
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Dana Nohynek, Director of Regulatory Affairs and Quality Assurance, provides an overview of how and why to manage risk in clinical trials.
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Project Manager Laura Zunino provides an overview of the informed consent process, why it matters, and how to improve it.
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