Global Regulatory Affairs Director, Oncology & ATMP

A biopharmaceutical company is seeking an Associate Director of Regulatory Affairs to develop global regulatory strategies for clinical programs. This role involves collaborating with health authorities for efficient approvals, managing regulatory submissions, and overseeing clinical trial compliance. Ideal candidates have over 8 years of experience in the industry with significant knowledge of biologics and international regulatory frameworks. This remote position requires alignment with core working hours in Eastern Time.
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