Biomarker Consent Specialist - Remote, Global Trials

A globally recognized Clinical Research Organization is seeking a Biomarker Consent Specialist to join their team in Oklahoma City. The role involves authoring, reviewing, and negotiating genetic language in clinical trial informed consents while managing multiple assignments in a fast-paced environment. Candidates must possess at least a Bachelor's degree and have a minimum of 5 years of experience with global clinical trials and genetic informed consents. Excellent communication and critical thinking skills are essential for success. #J-18808-Ljbffr