Human Subject Protection Specialist

Responsibilities: of the Human Subject Protection Specialist include: • Provide subject matter expertise on Human Subjects Protection (HSP) regulations and their application within clinical research. • Review clinical trial protocols, informed consent documents, and related research materials for regulatory and ethical compliance. • Conduct reviews of regulations, ethical guidance, and policies related to the protection of human subjects in research. • Develop and maintain informed consent templates, SOPs, internal guidance documents, and quality control procedures. • Support client projects related to human subjects protection, clinical research compliance, and process improvement initiatives. Qualifications: for the Human Subject Protection Specialist include: • Bachelor's degree in a scientific, healthcare, clinical research, or related field. • Experience in medical writing, scientific writing, regulatory writing, IRB activities, clinical site coordination, research documentation, regulatory affairs, or clinical research compliance. • Working knowledge of Human Subjects Protection regulations, including the Common Rule (45 CFR 46), informed consent requirements, and related clinical research regulations. • Proficiency with Microsoft Office Suite, including Word, Excel, PowerPoint, and Outlook. • Experience within a clinical research, healthcare, hospital, academic medical center, or research institution environment preferred. Compensation: for the Human Subject Protection Specialist includes: • Salary Range: $28.80 - $36.06/hr, depending on experience • Comprehensive Benefit Package: Cigna Medical/Dental/Vision, 401K, Sick Leave as Required by Law This job is open for applications on October 20th, 2026. Applications will be accepted for at least 30 days from the posting date.