Regulatory Affairs Lead, CMC (Gene Therapy)

A biopharmaceutical company is seeking an Associate Director of Regulatory Affairs to lead CMC compliance strategies and drive regulatory success. The candidate will provide expert guidance for multiple programs, monitor changes in the regulatory environment, and act as a primary point of contact for stakeholders. Preferred qualifications include at least 8 years of experience in regulatory drug development with a focus on CMC, alongside strong leadership and communication skills. This role is located in Research Triangle Park, NC and offers a collaborative work culture.
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