Senior Manager, Regulatory Affairs US Advertising and Promotion - Immunology - Hybrid

Location: Hybrid, with 3 days in the office and 2 days remotely, from hirify.global headquarters in Lake County, Illinois; Florham Park, New Jersey; or Irvine, California, United States.

Salary: $124,500–$236,500 per year in base compensation.

Company

hirify.global discovers and delivers medicines and healthcare solutions across immunology, oncology, neuroscience, and aesthetics.

What you will do

• Monitor government, industry, and trade association activities affecting pharmaceutical regulatory policies.
• Draft and finalize comments for regulators and trade associations and communicate regulatory developments to internal subject-matter experts.
• Oversee regulatory staff responsible for ensuring advertising and promotional materials comply with FDA requirements, the Code of Federal Regulations, PhRMA principles, and internal policies.
• Develop and guide implementation strategies for promotional activities across therapeutic areas.
• Present regulatory information to cross-functional stakeholders, including Marketing, Medical, Clinical, Legal, Sales Training, Managed Care, and Public Affairs.
• Manage, train, mentor, and support the development of regulatory professionals.

Requirements

• Bachelor’s degree in a relevant science or healthcare discipline and at least 7 years of relevant industry experience.
• Alternatively, a PharmD degree with at least 5 years of relevant industry experience is preferred.
• Experience in US Regulatory Affairs Advertising and Promotion.
• Experience working in a complex, matrixed environment with strong negotiation and communication skills.
• Experience in a management capacity is preferred.
• Ability to work on the stated hybrid schedule from one of the listed United States headquarters.

Culture & Benefits

• Paid time off, including vacation, holidays, and sick leave.
• Medical, dental, and vision insurance for eligible employees.
• 401(k) plan for eligible employees.
• Eligibility to participate in long-term incentive programs.
• Cross-functional work with regulatory, commercial, medical, legal, and public affairs stakeholders.