Neurocrine Biosciences
Regulatory Ad Promo Associate Director
Neurocrine Biosciences, San Diego, California, United States, 92189
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. About the Role: Serves as the lead reviewer for medical education and commercial advertising and promotional materials for product, disease state, and training/education 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 Ad/Promotion function. Proactively reviews regulatory promotional guidelines and untitled/warning 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 Ad/Promo 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 is responsible for conducting the regulatory review of materials for assigned products/programs intended for use by the field medical team Tracks and evaluates FDA guidance, policies, and the overall regulatory environment and must be able to assess and communicate potential risk and impact to Sr. Leadership Develops and maintains 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 Identifies and recommends/implements policy and/or process changes as needed in partnership with Director, Regulatory Ad/Promo Maintains standard operating procedures and department working practices Mentors and develops junior level team members Other duties as assigned Requirements:
BS/BA degree in Life/Health Sciences or related field and 10+ years of Regulatory Affairs experience at a biotech, pharmaceutical or device company, including significant experience in Advertising & Promotion process management OR Master’s degree in Life/Health Science or related field and 8+ years of similar experience as noted above Emerging as an internal thought leader with technical and/or business expertise Applies in-depth knowledge of own area of expertise to solve problems, with guidance from Director, Regulatory Ad/Promo on complex/high risk matters Applies expertise to manage critical projects and/or relationships Integrates analysis of business objectives and strategic direction to resolve problems and recommend solutions Has input into short-term strategy and may be involved in long-term strategy on a functional level Strong communications, problem-solving, analytical thinking, and influencing skills Demonstrated ability to work independently with minimal direction, including functional representation within teams and committees in order to attain group goals Proven track record and experience in Advertising & Promotional review committees with a thorough understanding of FDA guidance and regulations Extensive knowledge of electronic document management systems (e.g. Veeva Vault or similar) Advanced in Microsoft Office programs and Adobe Professional.
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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. About the Role: Serves as the lead reviewer for medical education and commercial advertising and promotional materials for product, disease state, and training/education 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 Ad/Promotion function. Proactively reviews regulatory promotional guidelines and untitled/warning 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 Ad/Promo 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 is responsible for conducting the regulatory review of materials for assigned products/programs intended for use by the field medical team Tracks and evaluates FDA guidance, policies, and the overall regulatory environment and must be able to assess and communicate potential risk and impact to Sr. Leadership Develops and maintains 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 Identifies and recommends/implements policy and/or process changes as needed in partnership with Director, Regulatory Ad/Promo Maintains standard operating procedures and department working practices Mentors and develops junior level team members Other duties as assigned Requirements:
BS/BA degree in Life/Health Sciences or related field and 10+ years of Regulatory Affairs experience at a biotech, pharmaceutical or device company, including significant experience in Advertising & Promotion process management OR Master’s degree in Life/Health Science or related field and 8+ years of similar experience as noted above Emerging as an internal thought leader with technical and/or business expertise Applies in-depth knowledge of own area of expertise to solve problems, with guidance from Director, Regulatory Ad/Promo on complex/high risk matters Applies expertise to manage critical projects and/or relationships Integrates analysis of business objectives and strategic direction to resolve problems and recommend solutions Has input into short-term strategy and may be involved in long-term strategy on a functional level Strong communications, problem-solving, analytical thinking, and influencing skills Demonstrated ability to work independently with minimal direction, including functional representation within teams and committees in order to attain group goals Proven track record and experience in Advertising & Promotional review committees with a thorough understanding of FDA guidance and regulations Extensive knowledge of electronic document management systems (e.g. Veeva Vault or similar) Advanced in Microsoft Office programs and Adobe Professional.
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