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Job Description
Join Jazz Pharmaceuticals as a Director of Global Medical and Promotional Regulatory Affairs, leading the review of promotional materials and ensuring regulatory compliance across oncology products. Drive impactful strategies that support business objectives while working collaboratively with various departments.
Key Responsibilities
Lead the promotional material review committee (PMRC) for assigned products/therapeutic areas
Provide input on decisions regarding promotional materials to satisfy FDA regulations and corporate standards
Serve as the Promotional Regulatory Affairs lead for new product launches
Manage regulatory aspects of promotional material review and approval
Lead interactions with FDA/OPDP for assigned products
Required Qualifications
B.S or B.A. degree in a scientific discipline or equivalent
Substantial pharmaceutical industry experience in regulatory affairs advertising and promotion
Strong understanding of FDA regulations and guidelines
Strong judgment and decision-making skills
Excellent collaboration, verbal and written communication skills
Preferred Qualifications
Advanced degree in a scientific discipline (e.g. PharmD)
Experience with Oncology and new product launch support
Benefits & Perks
Medical, dental and vision insurance401k retirement savings planFlexible paid vacationDiscretionary annual cash bonus or incentive compensationDiscretionary equity grants