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 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, endocrine and psychiatric disorders. The company’s diverse portfolio includes FDA-approved treatments for tardive dyskinesia, Parkinson’s disease, endometriosis* and uterine fibroids*, as well as clinical programs in multiple 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. *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 while working with cross-functional project teams (clinical project managers, research, preclinical/clinical pharmacology, biometrics, regulatory, drug safety, CMC), creation and execution of clinical development plans, and the development of strategies that will ultimately lead to approvals of Neurocrine's products. Provides expert medical advice to advance the development portfolio and helps the company navigate the complex drug development landscape. Works closely with Research and Preclinical Development to develop biomarker strategy necessary for the most effective evaluation of novel molecules in early clinical development. _ Your Contributions (include, but are not limited to): For assigned programs, develops clinical development strategies and accountable for the study design of clinical trials in Development, leading the preparation of clinical study synopses and being a major contributor to the writing of protocols, the design of data collection systems, interpretation of clinical data, and the preparation of final clinical study reports. Engages with external experts and organizations as needed to achieve these aims Represents Medical/Clinical on the cross-functional Program Team as the Program/Therapeutic Medical Lead. Accountable and responsible for the medical input to integrated development plans prepared by the Program Team and the clinical development plans that underpin them. Collaborate cross-functionally to support medical activities for clinical studies Provides medical leadership to the Program Team. Accountable and responsible for driving the execution of the clinical development plan Develops and implements study protocols in conjunction with a multidisciplinary Development Team Assists in the identification and selection of clinical investigators for clinical trials and maintains appropriate communication and professional relationships as Sponsor medical monitor/representative Conducts medical assessment and disposition of adverse events (in conjunction with Drug Safety physician) and evaluate safety of clinical compounds prior to and during ongoing clinical studies Oversees the clinical trials program in conjunction with Clinical Operations in accordance with NBI SOPs, Good Clinical Practice, and applicable regulations Identifies resource requirements, leads budget planning and personnel forecasting for clinical research programs; key contributor in the recruitment, training and development of the clinical teams, as well as identifying and selecting clinical consultants as needed Leads the analysis, interpretation, and presentation of results of assigned clinical studies to internal and external audiences Works with Medical Affairs and external opinion leaders to secure new collaborators and present trial results Interfaces with Research, Product Development and Business Development to assess new product opportunities, develop clinical research strategy and product development plans Other duties as assigned Requirements: MD or DO (or equivalent) degree in relevant clinical specialty for the therapeutic area required and 4 years clinical experience with broad bio/pharmaceutical/CRO industry experience in drug development Accredited residency training and board certification preferred Recognized Internal thought leader and deep clinical and clinical research expertise in neurological diseases Requires broad, deep and comprehensive expertise in leading-edge theories and techniques for functional area Applies ingenuity and creativity to problem analysis and resolution in complicated and/or novel situations Influences internal/external business and/or industry issues that have an impact on Neurocrine Strong mentoring skills and leadership abilities to supervise lower levels and/or lead indirect teams Proven ability to translate strategy into tactical plans and drive outcomes Must be flexible, adaptable, self-motivated, able to prioritize, and able to manage/progress a large volume of work with minimal supervision Strong interpersonal skills and outstanding collaborative skills; proven track record and success in building relationships and having scientific discourse with medical and scientific experts Outstanding oral and written communication skills, with close attention to detail; ability to translate complex scientific concepts into simple language tailored for different audiences Demonstrated success with project management Proficiency with word processing, spreadsheet, database, and presentation software and with filing (archiving) systems Deep knowledge and understanding of the drug development process including technical, business, and regulatory issues Proven track record working with regulatory agencies and providing clinical leadership for the filing of INDs, NDAs, or other similar government filings Strong knowledge of Good Clinical Practice, regulatory procedures relevant to investigational drug development Strong knowledge in translational medicine and biomarker evaluation, clinical study execution, regulatory requirements and documents, study design, biostatistics, data analysis, report writing, and scientific presentation of data Able to effectively operate in a multi-level matrix corporate environment, requiring interaction with, and/or direction of clinical research project teams, including physicians, scientists, monitors, administrative, regulatory, commercial, and consultant personnel Demonstrated success managing interactions with external CROs, consultants and other contract organizations, especially from the context of a small group Has successfully driven program strategy, launch and project management within Clinical Development Previous experience with developing and implementing policies and processes #LI-TM1 Neurocrine Biosciences is an EEO/AA/Disability/Vets 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 $270,000.00-$390,975.00. Individual pay decisions depend on various factors, such as primary work location, complexity and responsibility of role, job duties/requirements, and relevant experience and skills. In addition, this position offers an annual bonus with a target of 35% 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 caregiver/parental 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. OUR VALUES: PASSION: We are driven and love what we do. We are committed to our goals and to making a difference. INTEGRITY: We do the right thing for patients and our community. We take accountability. We speak up. COLLABORATION: We trust one another. We are inclusive. We are respectful. We are transparent. Together we succeed. INNOVATION: We seek and create optimal solutions. TENACITY: We do not quit. We adapt. We accomplish what others cannot. Come join our team during this exciting time of growth and opportunities! We are a top place to work. Neurocrine Biosciences was named one of the FORTUNE Best Workplaces in Biopharma™ 2023. We were also named a Great Place to Work® Certified company and were recognized on Great Place to Work’s Best Workplaces for Parents™ 2020 list. ©2023 Fortune Media IP Limited. All rights reserved. Used under license.