Biomarker Consent Specialist - Remote, Global Trials

A leading Clinical Research Organization is seeking a Biomarker Consent Specialist in Concord, NH. This role involves authoring and reviewing genetic and biomarker language in clinical trial informed consent documents, collaborating with global stakeholders, and ensuring compliance with company policies. The ideal candidate will have a Bachelor's degree and at least 5 years of experience with global clinical trials and informed consent negotiations. The position offers a collaborative environment with ample opportunities for professional growth. #J-18808-Ljbffr