Regulatory Affairs Senior AnalystJob Description: Our Senior Associate I (Regulatory Affairs Senior Analyst) is actively accountable for daily activities to ensure on-time business support such as (but not limited to): Elaboration of New Synthetic and New Biological medicines dossiers.Responsibilities:Responsible for the day-to-day activities and delivery of Global Regulatory Affairs support services.Management of clinical trial applications to Competent Authorities, Ethics Committees, and Regulatory Agencies.Research, review, and report on applicable global regulations.Job Summary: In the Global Regulatory Affairs (GRA) team, we have an opening for a Regulatory Manager for the Latin America (LATAM) region to coordinate and drive regulatory and advocacy activities for our Bioactives (biotechnology food, feed, and technical).About the Company: At Novo Nordisk, we don’t wait for change; we drive the change. We’re committed to promoting and being an equal opportunity workplace and act as an affirmative action employer.General Duties & Responsibilities:Monitors and communicates regulatory changes that impact products, services, and business activities.Maintains knowledge of applicable laws and regulations.Offers guidance on implementing regulatory changes.Communicates detailed requirements to stakeholders.
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