A leading biopharmaceutical company in Weston, Massachusetts is seeking an Associate Director for Global Regulatory Affairs. The role involves developing regulatory strategies for early-stage drug development, preparing submissions for clinical trials, and managing projects across multidisciplinary teams. Candidates should have a Master's in life sciences with 7-10 years of experience in regulatory affairs, particularly in immunology, oncology, or rare diseases. Strong communication and organizational skills are essential for success in this position.
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