Biomarker Consent Specialist - Remote, Global Trials

A leading Clinical Research Organization is looking for a Biomarker Consent Specialist in Dover, Delaware. In this role, you'll engage in authoring and reviewing informed consent documents related to genetic and biomarker research. You should have a Bachelor’s degree and a minimum of 5 years' experience with global clinical trials, particularly in genetic informed consents. The position offers opportunities for professional growth within a collaborative environment, excellent benefits, and a focus on work-life balance. #J-18808-Ljbffr