Project Management Specialist

Role: Project Management Specialist supporting cross-functional project coordination within Zevra Therapeutics' clinical and regulatory development teams. Objectives: ensure project timelines, milestones, and deliverables are tracked, communicated, and executed efficiently. Responsibilities: develop and maintain project plans, facilitate meetings, prepare status reports, manage risks/issues logs, and support process improvements. Qualifications: Bachelor's in Business, Life Sciences, or related; 2–5 years of project coordination or management experience, preferably in biopharma, biotech, or healthcare; strong organizational, communication, and cross-functional collaboration skills. Technical skills include proficiency in MS Office, project management tools (e.g., Smartsheet, MS Project, Asana), and document management systems. High-Value Details: supporting clinical, regulatory, medical affairs, and commercial teams; experience with biopharma project workflows; focus on efficient communication and risk mitigation across departments in a fast-paced, evolving environment. Location: unspecified; no travel requirements noted.