Associate Medical Affairs Director

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.

Neurocrine Biosciencesis 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, visitneurocrine.com, and follow the company onLinkedIn,XandFacebook. (*in collaboration with AbbVie)

About the Role:

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• 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 4 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

• PhD and 7+ years of experience with a combination of clinical practice experience and Medical Affairs or related pharmaceutical consulting capacity OR

• PharmD and 7+ years of experience with a combination of clinical practice experience and Medical Affairs or related pharmaceutical consulting capacity

• MD preferred and 2+ years of relevant experience Preferred experience: Clinical Practice experience in Endocrinology

• Effective communicator with good team collaboration skills. Passion for education and addressing unmet medical needs in Endocrinology

• Strong knowledge in Endocrinology preferred

• Comprehensive knowledge of Good Clinical Practices (GCP), ICH, ICJME Guidelines, FDA and other international regulatory body requirements

• Experience in proactively engaging internal and external leaders while serving as the medical affairs representative for assigned programs

• Understands the connection of clinical, medical, and business needs

• Knowledge of aligning business and scientific goals and objectives

• Working knowledge of budget development

• Proven project management, and problem-solving skills

• Analytical, problem-solving, and decision-making skills oriented toward quality work and consistent attention to detail

• Strong writing abilities in the scientific or medical field

• Uses professional concepts in developing resolution to critical issues and broad design matters

• Expertise in developing policies and processes

• Recognized as an internal thought leader with extensive technical and business expertise within a strategic organization

• Applies in-depth knowledge of own function, business / commercial / scientific expertise to solve critical issues successfully and innovatively

• Evaluates key business / scientific challenges and completes complex, ambiguous initiatives having cross-functional impact

• Strong interpersonal and communication skills as well as strong organizational and team leadership skills are required

• Able to work independently and prioritize multiple tasks and goals to ensure the timely, on-target and within-budget accomplishment

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Neurocrine Biosciences is an EEO/Disability/Vets employer.

We are committed to building a workplace of belonging, respect, and empowerment, 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.

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