A biopharmaceutical company in Boston seeks a Regulatory Affairs Manager to oversee submission processes and maintain compliance for drug filings. Candidates should have over 8 years in regulatory documentation and operations in pharma or biotech, alongside at least 5 years in a management role. Essential skills include expertise in eCTD submissions and strong proficiency in MS Office tools. The role may involve some international travel and offers a comprehensive benefits package including health and retirement plans.
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