Associate Medical Affairs Director

About the role

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. What We Do: Neurocrine Biosciences is a leading neuroscience-focused, biopharmaceutical company with a simple purpose: to relieve suffering for people with great needs. 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, classic congenital adrenal hyperplasia, 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 neurocrine.com , and follow the company on LinkedIn , X and Facebook . ( *in collaboration with AbbVie ) Responsible for the development of medical affairs strategy, planning, and tactical implementation for all medical affairs functions including publication planning, data generation and communication, KOL interactions, knowledge management, medical education, advisory boards, and cross-functional partnership. Will travel to congresses and other external meetings as necessary. _ Your Contributions (include, but are not limited to): Medical Affairs Planning Partner with key cross-functional stakeholders to develop strategic and aligned Medical Affairs Plans for therapeutic areas of interest Assists in communication and represents plans within the organization. Continuously update plans and inform stakeholders of progress Collaboratively develop a fully referenced scientific platform and lexicon supporting the foundational understanding of Neurocrine therapeutic platforms, describing their derivation, MOA, multimodal attributes and potential for treating various disorders with unmet medical need Assist in gaining the endorsement of the platform from internal and external opinion leaders and educate the organization on its content and use Data Generation Aid in establishing strategically aligned key areas of interest for IIS, collaborative research agreements and Phase IV clinical trials Direct and design collaborative research and Phase IV clinical trials for assigned area May serve on review committees for review and approval of investigator initiated and medical education grant requests Provide medical input into clinical development and lifecycle management activities Collaborate with Clinical Development to support clinical trials and pipeline programs Data Communication Develop and execute strategically aligned publication plans for key therapeutic areas in collaboration with Medical Communications Participate in congress planning including medical education, competitive intelligence Establish working relationships with KOLs and payers to understand the therapeutic landscape, data gaps and areas of educational unmet needs and garner feedback on key programs Scientific and Medical Consultant to Internal Stakeholders, may be asked to consult External Stakeholders Serve as Medical/Scientific Subject Matter Expert Provide knowledge and expertise for assigned products including (but not limited to) PRC, health outcomes plans, MSL activities, speaker programs, training, CME grant reviews or other internal key business processes