Associate Director, Regulatory Ad/Promo
Neurocrine Biosciences - san diego, CA
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Who We Are:At Neurocrine Biosciences, we pride ourselves on having a strong, inclusive, and positive culture based on our shared purpose and values. We know what it takes to be great, and we are as passionate about our people as we are about our purpose - to relieve suffering for people with great needs, but few options.What We Do:Neurocrine Biosciences is a leading neuroscience-focused, biopharmaceutical company with a simple purpose: to relieve suffering for people with great needs, but few options. We are dedicated to discovering and developing life-changing treatments for patients with under-addressed neurological, neuroendocrine, and neuropsychiatric disorders. The company's diverse portfolio includes FDA-approved treatments for tardive dyskinesia, chorea associated with Huntington's disease, endometriosis* and uterine fibroids*, as well as a robust pipeline including multiple compounds in mid- to late-phase clinical development across our core therapeutic areas. For three decades, we have applied our unique insight into neuroscience and the interconnections between brain and body systems to treat complex conditions. We relentlessly pursue medicines to ease the burden of debilitating diseases and disorders, because you deserve brave science. For more information, visit , and follow the company on LinkedIn, X (Formerly Twitter) and Facebook. (*in collaboration with AbbVie)About the Role:Serves as the lead reviewer for medical education and commercial advertising and promotional materials for product, disease state, and trainingeducation programs. Leads cross-functional collaboration to ensure appropriate reviews take place and timely submissions are made to OPDP. Work closely with the Director, Regulatory Ad Promo to formulate the strategic direction and develop process improvements for the Regulatory AdPromotion function. Proactively reviews regulatory promotional guidelines and untitledwarning letters; assesses phase IV clinical trial design with regard to possibilities for use in proactive or reactive marketing or medical communication. Assesses labeling changes for potential impact on AdPromo and and medical communications materials.Your Contributions (include, but are not limited to):Assumes a leadership role in the PRC Process for assigned products to ensure compliance with FDA advertising and promotional regulations and guidelines for select product, disease state, and all medical education materials.Responsible for timely and accurate review, and timely submission of promotional materials (i.e. FDA 2253 submissions).Independently represents Regulatory Affairs on the Medical Review Committee (MRC) and be responsible for conducting the regulatory review of materials for assigned productsprograms intended for use by the field medical team.Track and evaluate FDA guidance, policies and the overall regulatory environment and must be able to assess and communicate potential risk and impact to Sr. Leadership.Develop and maintain a business partnership environment between Regulatory Affairs, PRC and MRC partner functions in the review and approval of advertising and promotional materials.Actively manages communications to Regulatory management, and ensures promotional claims are in compliance with terms of approved product registrations, current labeling, applicable laws, internal policies and external regulations.Proactively assesses advertising and promotion-related processes and procedures to enhance efficiencies and compliance.Identify and recommendimplement policy andor process changes as needed in partnership with Director, Regulatory AdPromo.Maintain standard operating procedures and department working practices.Mentors and develops junior level team members.Other duties as assigned.Requirements:BSBA degree in LifeHealth Sciences or related field and 10+ year's of Regulatory Affairs experience at a biotech, pharmaceutical or device company, including significant experience in Advertising & Promotion process management ORMaster's degree in LifeHealth Science or related field and 8+ years of similar experience as noted aboveEmerging as an internal thought leader with technical andor business expertiseApplies in-depth knowledge of own area of expertise to solve problems, with guidance from Director, Regulatory AdPromo on complexhigh risk mattersApplies expertise to manage critical projects andor relationshipsIntegrates analysis of business objectives and strategic direction to resolve problems and recommend solutionsHas input into short-term strategy and may be involved in long-term strategy on a functional levelStrong communications, problem-solving, analytical thinking, influencing skillsDemonstrated ability to work independently with minimal direction, including functional representation within teams and committees in order to attain group goalsProven track record and experience in Advertising & Promotional review committees with a thorough understanding of FDA guidance and regulationsExtensive knowledge of electronic document management systems (e.g. Veeva Vault or similar)Advanced in Microsoft Office programs and Adobe Professional.Neurocrine Biosciences is an EEOAADisabilityVets employer.We are committed to building a diverse, equitable, and inclusive workplace, and we recognize there are a variety of ways to meet our requirements. We are looking for the best candidate for the job and encourage you to apply even if your experience or qualifications don't line up to exactly what we have outlined in the job description.The annual base salary we reasonably expect to pay is $167,000.00-$241,925.00. Individual pay decisions depend on various factors, such as primary work location, complexity and responsibility of role, job dutiesrequirements, and relevant experience and skills. In addition, this position offers an annual bonus with a target of 30% of the earned base salary and eligibility to participate in our equity based long term incentive program. Benefits offered include a retirement savings plan (with company match), paid vacation, holiday and personal days, paid caregiverparental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage in accordance with the terms and conditions of the applicable plans.
Created: 2024-11-02