Biomarker Consent Specialist - Remote, Global Trials

A leading Clinical Research Organization is seeking a Biomarker Consent Specialist to join their team in Lansing, Michigan. The role involves authoring, reviewing, and negotiating genetic and biomarker language in clinical trial informed consent documents. Candidates must have at least a bachelor's degree and a minimum of 5 years' experience in global clinical trials. They will collaborate with internal and external teams to ensure compliance and consistency in informed consent language, all while enjoying a flexible work environment. #J-18808-Ljbffr