Neurocrine Biosciences
Sr. Medical Director, MD- (Neuropsychiatry)
Neurocrine Biosciences, New London, Connecticut, us, 06320
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. 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) About the Role:
Medical expert responsible for the development of clinical research strategies and independent direction of Phase 1-3 clinical studies in the Neuropsychiatry therapeutic area while working with cross-functional project teams (clinical project managers, preclinical/clinical pharmacology, biometrics, regulatory, drug safety). Creation and execution of clinical development plans and strategies that will ultimately lead to product approvals. Provide expert medical advice to advance the development portfolio and help navigate the complex drug development landscape. Collaborate closely with Research and Preclinical Development to develop biomarkers for effective evaluation of novel molecules in early clinical development. Your Contributions (include, but are not limited to):
Develop clinical development strategies and be accountable for study design of clinical trials, including preparation of study synopses, protocol writing, data collection system design, data interpretation, and final report preparation. Engage with external experts as needed. Represent Medical/Clinical on the Program Team as the Medical Lead. Provide medical input to development plans and support medical activities for clinical studies. Provide medical leadership to the Program Team and drive the execution of the clinical development plan. Develop and implement study protocols with the Development Team. Assist in selecting clinical investigators and maintain professional relationships as Sponsor medical monitor/representative. Conduct medical assessments and manage adverse events, evaluating safety during clinical studies. Oversee clinical trials in conjunction with Clinical Operations, ensuring compliance with SOPs, GCP, and regulations. Identify resource needs, lead budget and personnel planning, and contribute to team recruitment and training. Lead analysis, interpretation, and presentation of clinical study results to various audiences. Work with Medical Affairs and external opinion leaders to secure collaborations and present results. Interface with Research, Product Development, and Business Development for new product opportunities and strategies. Perform other duties as assigned. Requirements:
MD or DO (or equivalent) degree with 4+ years of clinical experience and industry experience in drug development. Residency training and board certification preferred. Recognized thought leader with deep expertise in a relevant discipline. Broad, deep expertise in leading-edge theories and techniques. Ability to solve complex problems creatively. Influence industry and business issues impacting Neurocrine. Strong mentoring and leadership skills. Ability to translate strategy into tactical plans and drive outcomes. Flexible, self-motivated, and able to prioritize effectively. Excellent interpersonal and collaborative skills. Outstanding communication skills, with ability to simplify complex concepts. Proven project management success. Proficiency in common software tools and filing systems. Deep knowledge of drug development, regulatory issues, and clinical research processes. Experience working with regulatory agencies and leading filings. Strong knowledge of GCP, regulatory procedures, translational medicine, and biomarker evaluation. Ability to operate effectively in a matrix environment involving diverse teams. Experience managing external CROs and external partnerships. Successful track record in program strategy, launch, and project management within Clinical Development. #LI-SW1 Neurocrine Biosciences is an EEO/Disability/Vets employer. We are committed to building a workplace of belonging, respect, and empowerment. We encourage applications from candidates of diverse backgrounds, even if your experience doesn’t perfectly match every requirement. The expected annual base salary range is $290,300.00 - $420,250.00, depending on various factors including location, experience, and skills. The position offers an annual bonus target of 35%, participation in our long-term incentive program, and benefits including a retirement plan, paid leave, and health coverage.
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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. 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) About the Role:
Medical expert responsible for the development of clinical research strategies and independent direction of Phase 1-3 clinical studies in the Neuropsychiatry therapeutic area while working with cross-functional project teams (clinical project managers, preclinical/clinical pharmacology, biometrics, regulatory, drug safety). Creation and execution of clinical development plans and strategies that will ultimately lead to product approvals. Provide expert medical advice to advance the development portfolio and help navigate the complex drug development landscape. Collaborate closely with Research and Preclinical Development to develop biomarkers for effective evaluation of novel molecules in early clinical development. Your Contributions (include, but are not limited to):
Develop clinical development strategies and be accountable for study design of clinical trials, including preparation of study synopses, protocol writing, data collection system design, data interpretation, and final report preparation. Engage with external experts as needed. Represent Medical/Clinical on the Program Team as the Medical Lead. Provide medical input to development plans and support medical activities for clinical studies. Provide medical leadership to the Program Team and drive the execution of the clinical development plan. Develop and implement study protocols with the Development Team. Assist in selecting clinical investigators and maintain professional relationships as Sponsor medical monitor/representative. Conduct medical assessments and manage adverse events, evaluating safety during clinical studies. Oversee clinical trials in conjunction with Clinical Operations, ensuring compliance with SOPs, GCP, and regulations. Identify resource needs, lead budget and personnel planning, and contribute to team recruitment and training. Lead analysis, interpretation, and presentation of clinical study results to various audiences. Work with Medical Affairs and external opinion leaders to secure collaborations and present results. Interface with Research, Product Development, and Business Development for new product opportunities and strategies. Perform other duties as assigned. Requirements:
MD or DO (or equivalent) degree with 4+ years of clinical experience and industry experience in drug development. Residency training and board certification preferred. Recognized thought leader with deep expertise in a relevant discipline. Broad, deep expertise in leading-edge theories and techniques. Ability to solve complex problems creatively. Influence industry and business issues impacting Neurocrine. Strong mentoring and leadership skills. Ability to translate strategy into tactical plans and drive outcomes. Flexible, self-motivated, and able to prioritize effectively. Excellent interpersonal and collaborative skills. Outstanding communication skills, with ability to simplify complex concepts. Proven project management success. Proficiency in common software tools and filing systems. Deep knowledge of drug development, regulatory issues, and clinical research processes. Experience working with regulatory agencies and leading filings. Strong knowledge of GCP, regulatory procedures, translational medicine, and biomarker evaluation. Ability to operate effectively in a matrix environment involving diverse teams. Experience managing external CROs and external partnerships. Successful track record in program strategy, launch, and project management within Clinical Development. #LI-SW1 Neurocrine Biosciences is an EEO/Disability/Vets employer. We are committed to building a workplace of belonging, respect, and empowerment. We encourage applications from candidates of diverse backgrounds, even if your experience doesn’t perfectly match every requirement. The expected annual base salary range is $290,300.00 - $420,250.00, depending on various factors including location, experience, and skills. The position offers an annual bonus target of 35%, participation in our long-term incentive program, and benefits including a retirement plan, paid leave, and health coverage.
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