Nonclinical Regulatory Specialist

Partnering with nonclinical scientists and regulatory stakeholders, the full-time remote Nonclinical Regulatory Specialist will coordinate activities to support regulatory readiness of nonclinical deliverables throughout the product lifecycle. Key responsibilities Coordinate activities for nonclinical regulatory planning, document development, and regulatory readiness Develop and maintain integrated timelines for nonclinical regulatory documents and deliverables Facilitate cross-functional planning meetings and track progress on action items and commitments Required qualifications Master's degree and 1 year of directly related experience, or Bachelor's degree and 5 years, or Associate's degree and 10 years of directly related experience Experience supporting pharmaceutical research and development or nonclinical drug development programs Understanding of nonclinical drug development and regulatory requirements Demonstrated project or program management skills, including timeline development and risk management Familiarity with Good Laboratory Practice (GLP) and global regulatory expectations for nonclinical documentation