A leading pharmaceutical company in New Mexico is seeking a senior regulatory leader to oversee regulatory affairs for vaccines and anti-infectives. The candidate must hold an MD, PhD, or PharmD and have at least 10 years of regulatory experience. This hybrid role requires on-site presence an average of 2.5 days a week. Responsibilities involve global resource allocation, staff management, and ensuring governance in regulatory projects. This role promises an impactful contribution to developing patient-focused solutions.
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