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Associate Director, Regulatory Project Management

Job Type

Permanent

Employment

Full Time

8 years of Regulatory affairs experience with in Pharm/biotech

Job Responsibilities

Regulatory Project Management

Qualifications

    • 8 years of Regulatory affairs experience with in Pharm/biotech
    • Experience managing US and EMA regulatory submissions
    • Collaborate with clinical and CMC regulatory leaders to author regulatory documents
    • Experience with regulatory filings across the biological product lifecycle – investigational product through application for licensure
    • Location DMV-Open to remote candidates
    • $155,000-180,000 plus bonus and options
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February 19, 2025