7 дней назад
Senior Manager Regulatory Affairs Advertising and Promotion
122 250 - 176 583$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Senior Manager Regulatory Affairs Advertising and Promotion (Pharmaceutical Advertising and Promotion): Conducting independent regulatory reviews of advertising, promotional, and communications materials while developing strategies for product launches, labeling, and product defense with an accent on FDA compliance, risk-benefit analysis, and cross-functional collaboration. Focus on leading promotional review committees, advising commercial and medical teams, and managing regulatory strategies for pharmaceutical products.
Location: Hybrid role based in Morristown, New Jersey or Cambridge, Massachusetts; available to US and Puerto Rico residents only.
Salary: $122,250.00–$176,583.33 per year.
Company
is an R&D-driven biopharmaceutical company developing medicines and vaccines through immunoscience, AI, data, and digital platforms.
What you will do
- Conduct independent regulatory reviews of advertising, promotional, communications, commercial, and medical materials.
- Develop and implement regulatory strategies for advertising campaigns, product launches, labeling, product defense, and development projects.
- Identify advertising and promotion issues, assess risk-benefit options, and recommend solutions to cross-functional stakeholders.
- Represent Regulatory Affairs on brand teams and review committees for commercial and medical materials.
- Provide guidance to commercial, medical, R&D, and global teams on product development, promotion, advertising, reimbursement, and lifecycle management.
- Serve as the primary liaison with the FDA on advertising and promotional compliance matters for assigned products.
Requirements
- Bachelor’s degree from an accredited four-year college or university; a science focus is preferred.
- At least 3 years of experience in pharmaceutical or medical device advertising and promotional review.
- Ideally 1–3 years of relevant regulatory experience and experience working with Medical, Legal, Marketing, and other cross-functional groups.
- Knowledge of complex medical and scientific subjects, medical terminology, and the US pharmaceutical marketplace.
- Strong written and oral communication, analytical, prioritization, multitasking, and project management skills.
- Professional integrity, sound judgment, and the ability to build collaborative internal networks.
Culture & Benefits
- Work alongside a supportive, future-focused team advancing biopharmaceutical research.
- Access career growth opportunities through promotions and lateral moves in the US and internationally.
- Receive health and wellbeing benefits, including healthcare, prevention and wellness programs, and at least 14 weeks of gender-neutral parental leave.
- Contribute to drug development informed by patient insights and supported by AI, data, and digital platforms.
- Participate in employee benefit programs and a rewards package aligned with experience and contribution.
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