Associate Director, Regulatory Affairs, Advertising, Promotion & Labeling (RA-APL)

Why Join Intellia? Our mission is to develop curative genome editing treatments that can positively transform the lives of people living with severe and life-threatening diseases. Beyond our science, we live our four core values: One, Explore, Disrupt, Deliver and feel strongly that you can achieve more at Intellia. We have a single-minded determination to excel and succeed together. We believe in the power of curiosity and pushing boundaries. We welcome challenging thoughts and imagination to develop innovative solutions. And we know that patients are counting on us to make the promise a reality, so we must maintain high standards and get it done. We want all of our people to go beyond what is possible. We aren't constrained by typical end rails, and we aren't out to just "treat" people. We're all in this for something more. We're driven to cure and motivated for change. Just imagine the possibilities of what we can do together. How You Will Achieve More: The Associate Director, Regulatory Affairs Advertising, Promotion & Labeling (AD RA-APL) provides regulatory advertising and promotion guidance for compliant external communications. This role works closely with commercial/launch teams, medical affairs, research and development, corporate communications, and legal to ensure external communications, including but not limited to promotional communications, are compliant with regulatory requirements and align with strategic objectives and commercial regulatory strategy. Develops innovative and compliant strategies to support advertising & promotion objectives Represents Regulatory on the Commercial Medical, Legal, Regulatory Committee (CMLR) to navigate claims and presentations, providing advice based on the Federal Food, Drug, & Cosmetic Act (FDCA) and implementing regulations impacting advertising & promotional labeling Thinks innovatively and creatively, identifying the risks surrounding promotional claims and campaigns Manages the FDA 2253 program, leading submission of branded promotional materials to FDA Advertising & Promotional Labeling Branch (APLB) and/or Office of Prescription Drug Promotion (OPDP) at time of initial dissemination by Commercial Represents Regulatory on the Medical Review Committee (MRC) and Scientific Communications Review Committee (SCRC) Experience with developing product labeling and knowledge of labeling regulations a plus Responsibilities: Interprets content of FDA regulations, guidance documents, and enforcement letters and communicates information to stakeholders in order to ensure compliant commercial materials Accountable for review and approval of materials for both promotion and scientific exchange, in line with relevant goals and deliverables with a broad impact on the organization Proposes creative, effective and compliant regulatory strategies and solutions to promotional concepts that meet business objectives and minimize risk Provides promotional regulatory input on concepts and draft materials to ensure they are aligned with promotional regulations, corporate standards and policies and business objectives Primary Regulatory Advertising & Promotion contact for Regulatory Agencies Manages contracted submission coordinator and publisher related to FDA 2253 program Maintains current awareness of evolving FDA regulations and interpretations, FDA advisory letters, enforcement letters and policy issues affecting the pharmaceutical/biologics industry Solid understanding of pharmaceutical regulatory affairs, and knowledge of fundamentals of labeling regulatory requirements and industry practice. Exceptional understanding of medical concepts and terminology, and strong written and oral communication skills, including presentation skills. Strong aptitude for use of electronic systems to support Regulatory reviews and submissions. About You: In-depth understanding of regulatory advertising and promotional labeling concepts Consistent track record of advising on successful business strategies for branded and unbranded promotional campaigns Strong ability to work independently, with flexibility, and to collaborate with stakeholders Previous working knowledge of FDA 2253 program Experience in managing complex projects. Demonstrated ability to work with people in a global, dynamic environment to deliver value-added results. Solid ability to recognize and escalate issues. Capable of dealing with ambiguity. Creative and comfortable working with multifunctional teams. Strong interpersonal skills. Proven negotiator and demonstrated ability to use constructive debate to identify and move others towards compliant promotional outcomes. Well organized with exceptional communication skills, strong influencing skills, strong technical writing and documentation skills, as well as strong analytical and problem-solving skills Proficient in computer applications and configurations including Microsoft Office Suite or related software, and electronic document management systems (e.g., Veeva Vault PromoMats and MedComms) Product launch experience is a plus BS degree in scientific, clinical or related area required. Advanced degree highly desirable. Regulatory Affairs Certification is a plus 6+ years pharmaceutical/biotech industry experience with a minimum of 4 years of direct experience as Regulatory reviewer of advertising and promotional materials is required. Demonstrated history of successful interactions with promotional review divisions of FDA (OPDP/APLB) Prolonged periods of sitting at a desk and working on a computer. #LI-Remote EEOC Statement: Intellia believes in a diverse environment, and is committed to equal employment opportunity for all its employees and qualified applicants. We do not discriminate in recruitment, hiring, training, promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. Intellia will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law. Applications are accepted on a rolling basis, and will continue to be accepted until the position is filled at which point the position will be taken down. The base salary for this position is expected to range between $193,176.00 - $236,104.00 USD per year. The salary offered is determined based on a range of factors including, but not limited to, relevant education and training, overall related experience, specialized, rare or in-demand skill sets, internal comparators and other business needs. Upon joining Intellia, your salary will be reviewed periodically and additional factors such as time in role and performance will be considered. Intellia may change the published salary range based on company and market factors. Additional compensation includes a performance-based annual cash bonus, a new hire equity grant, and eligibility to be considered for annual equity awards the value of which are determined annually at the Company's discretion. For more information about Intellia's benefits, please click here. At Intellia, we are committed to solving the complex challenges of making CRISPR/Cas9-based medicines a reality for patients suffering from genetic diseases and to create novel engineered cell therapies for immuno-oncological and autoimmune diseases.