Job Description:
• Lead the regulatory evaluation of IRB research protocols by the Human Subjects Protection Program
• Advise and educate the IRB as well as researchers regarding regulatory, legal, and other requirements of research protocols
• Lead various efforts to develop and define the human subjects' protection program
• Make pivotal contributions to research compliance efforts to assess and mitigate research compliance risks
• Support various Research Institute initiatives
Requirements:
• Bachelor's Degree OR significant/applicable college coursework that demonstrates competency
• At least five (5) years of related experience including IRB, medical research, or legal/regulatory experience
• Progressively responsible experience in a professional setting
• Juris Doctor from an accredited law school OR PhD or higher level of advanced science degree (preferred)
• License to practice law in the State of Washington (preferred)
• Eight (8) or more years of related experience including IRB, medical research, or legal/regulatory experience (preferred)
• Knowledge of FDA-regulated research (preferred)
Benefits:
• medical, dental, and vision plans
• 403(b)
• life insurance
• paid time off
• tuition reimbursement
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