Iovance Biotherapeutics is seeking an Associate Director of Regulatory Affairs to lead drug development programs. This role involves managing interactions with regulatory authorities and overseeing clinical-regulatory document creation. The ideal candidate has significant experience in oncology drug development and a strong background in regulatory strategy.

Minimum 10 years in regulatory affairs is required, and candidates should be skilled in document creation and project management. A collaborative approach and strong communication skills are essential for success within this dynamic team.
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