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1 Vacancy
The Role:
The Manager Global Regulatory Advertising and Promotion will be responsible for ensuring compliance with regulatory requirements for promotional and nonpromotional materials across various communication channels. This role will serve as a key liaison between Regulatory Affairs Legal Medical and Commercial teams to provide strategic regulatory guidance on advertising and promotional activities. The ideal candidate will have expertise in FDA regulations OPDP (Office of Prescription Drug Promotion)/Advertising and Promotional Labeling Branch (APLB) guidance and industry best practices.
Heres What Youll Do:
Regulatory Compliance & Review:
Review and approve promotional materials corporate communications and disease awareness campaigns to ensure compliance with FDA and other applicable regulatory requirements.
Maintain uptodate knowledge of regulatory requirements enforcement trends and industry best practices.
CrossFunctional Collaboration:
Act as a key member of the Promotional Material Review Team (PMRT) and Medical Review Committee (MRC) working closely with Marketing Medical Legal and Compliance teams to develop impactful material that aligns with regulatory expectations.
Summarize FDA enforcement actions for key stakeholders at Moderna
Health Authority Interactions:
Support interactions with the FDAs Advertising and Promotional Labeling Branch (APLB) and other regulatory authorities as needed.
Prepare regulatory submissions for promotional materials including 2253 filings and advisory comments requests.
Training & Process Improvement:
Assist with developing training programs on promotional regulations for internal stakeholders.
Help refine internal SOPs best practices and review processes for advertising and promotion compliance.
Monitor and analyze enforcement actions and industry trends to proactively mitigate regulatory risks.
Heres What Youll Need:
Education:
Bachelors degree in a relevant field (e.g. Life Sciences Pharmacy Regulatory Affairs or a related discipline).
Advanced degree (PharmD JD or Masters in Regulatory Affairs) preferred.
Experience:
Minimum 2 years of experience in Regulatory Affairs with at least 1 year focused on advertising and promotion in the pharmaceutical biotech or medical device industry.
Strong knowledge of applicable regulations and enforcement trends
Prior experience working with crossfunctional review committees in a regulated environment.
Global regulatory knowledge (EMA Health Canada etc.) is a plus.
Skills & Competencies:
Understanding of US and global regulatory frameworks for advertising and promotion.
Excellent ability to interpret and apply regulatory guidelines and requirements in a businessfocused solutionsoriented manner.
Strong written and verbal communication skills with experience in preparing regulatory documentation.
Ability to work crossfunctionally and manage multiple projects in a fastpaced environment.
Strong attention to detail and problemsolving skills.
Heres What Youll Bring to the Table:
Familiarity with digital and social media promotional compliance.
Experience in infectious diseases oncology rare diseases and/or vaccines is a plus.
At Moderna we believe that when you feel your best you can do your best work. Thats why our US benefits and global wellbeing resources are designed to support youat work at home and everywhere in between.
About Moderna
Since our founding in 2010 we have aspired to build the leading mRNA technology platform the infrastructure to reimagine how medicines are created and delivered and a worldclass team. We believe in giving our people a platform to change medicine and an opportunity to change the world.
By living our mission values and mindsets every day our people are the driving force behind our scientific progress and our culture. Together we are creating a culture of belonging and building an organization that cares deeply for our patients our employees the environment and our communities.
We are proud to have been recognized as a Science Magazine Top Biopharma Employer a Fast Company Best Workplace for Innovators and a Great Place to Work in the U.S.
If you want to make a difference and join a team that is changing the future of medicine we invite you to visit to learn more about our current opportunities.
Our Working Model
As we build our company we have always believed an inperson culture is critical to our success. Moderna champions the significant benefits of inoffice collaboration by embracing a 70/30 work model. This 70% inoffice structure helps to foster a culture rich in innovation teamwork and direct mentorship. Join us in shaping a world where every interaction is an opportunity to learn contribute and make a meaningful impact.
Moderna is a smokefree alcoholfree and drugfree work environment.
Equal Opportunities
Moderna is committed to equal employment opportunity and nondiscrimination for all employees and qualified applicants without regard to a persons race color sex gender identity or expression age religion national origin ancestry or citizenship ethnicity disability military or protected veteran status genetic information sexual orientation marital or familial status or any other personal characteristic protected under applicable is a place where everyone can grow. If you meet the Basic Qualifications for the role and you would be excited to contribute to our mission every day please apply!
Moderna is an EVerify Employer in the United States. We consider qualified applicants regardless of criminal histories consistent with legal requirements.
Accommodations
Were focused on attracting retaining developing and advancing our employees. By cultivating a workplace that values diverse experiences backgrounds and ideas we create an environment where every employee can contribute their best.
Moderna is committed to offering reasonable accommodations to qualified job applicants with disabilities. Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should contact the Accommodations team at .
Export Control Notice
This position may involve access to technology or data that is subject to U.S. export control laws including the Export Administration Regulations (EAR). As such employment is contingent upon the applicants ability to access exportcontrolled information in accordance with U.S. law. Due to the nature of the work and regulatory requirements only individuals who qualify as U.S. persons (citizens permanent residents asylees or refugees) are eligible for this position. For this role Moderna is unable to sponsor nonU.S. persons to apply for an export control license.
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