CSL is transforming its R&D organization to accelerate innovation and create greater impact for patients. With a streamlined, project-led structure and a focus on collaboration, we're building a future-ready team that excels in dynamic biotech ecosystems. Joining CSL now means being part of an agile team committed to developing therapies that make a meaningful difference worldwide.
Could you be our next Senior Manager US Advertising and Promotion Lead? The job is in our King of Prussia, PA, Waltham MA, Zurich Switzerland or Maidenhead UK office. This is a hybrid position and is onsite three days a week. You will report to the Head, Global Advertising & Promotional
Position Purpose
1. Provide an overview of the responsibilities of the position by summarizing the most important aspects and duties.
2. Ensure compliance with HA drug promotion and promotional labeling regulations for assigned licensed products.
3. Review, approve, or reject promotional programming based on U.S. Code of Federal Regulations and FDA implementing regulations and guidance.
4. Adhere to related SOPs and work instructions for established MCC/PRC processes.
Main Responsibilities and Accountabilities
5. Review advertising and promotional labeling; comment, improve, approve, or reject material based on company practice, CSL policy, U.S. law, and FDA regulations.
6. Collaborate with Commercial Operations Marketing, Legal, and Medical personnel to minimize HA enforcement risk while supporting CSL’s commercial success.
7. Monitor and apply trends in advertising and promotional labeling regulations to CSL U.S. regional review practices and processes.
8. Provide regulatory leadership and guidance to marketing during development, review, and approval of promotional materials for assigned therapeutic areas.
9. Prepare and submit advertising and promotional labeling materials to the FDA as required under 21 CFR 314.81(b)(3)(i) or 21 CFR 601.45.
10. Maintain technical biologics/medical knowledge for assigned therapeutic areas.
11. Actively contribute to the global CSL regulatory community through designated projects and assignments.
12. Review and advise product development teams on communication strategies or tactics regarding investigational products.
Experience
13. Bachelor's Degree Life Science
14. Minimum 3 years in Regulatory, Medical, or Legal Affairs or other relevant experience.
15. Skilled in implementing regulatory science and monitoring enforcement trends.
16. Ability to read and comprehend product-related technical and medical information.
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About CSL Behring
CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients’ needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives.
CSL Behring operates one of the world’s largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries.
To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit and CSL Plasma at .
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