Biomarker Consent Specialist - Remote, Global Trials

A leading Clinical Research Organization is looking for a Biomarker Consent Specialist in Cheyenne, Wyoming. This role involves authoring and reviewing genetic language in trial informed consents, working independently and collaboratively in a fast-paced environment. Candidates should have a BA/BS and at least 5 years of experience with global clinical trials and genetic informed consents. The position supports a culture of collaboration and offers growth opportunities. Benefits include health insurance, tuition reimbursement, and 401(k) match. #J-18808-Ljbffr