Madrigalpharma
A biopharmaceutical company is seeking an experienced Regulatory Affairs professional to manage day-to-day regulatory activities. The ideal candidate will have 8-10 years of experience in pharmaceutical drug development, excellent communication and negotiation skills, and a strong understanding of regulatory guidelines. Responsibilities include collaborating with various departments on labeling and submissions while acting as the liaison with regulatory agencies. A strong regulatory background and strategic thinking are essential for this role, based in Conshohocken, PA or Waltham, MA.
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