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Neurocrine Biosciences

Develops and markets neurology-focused therapies

Executive Director - Regulatory Strategy

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeSan Diego, CA, USAIn-person

About the Job

Requirements

  • A Bachelor of Science or Bachelor of Arts degree in a life science and a second Bachelor of Science or Bachelor of Arts degree, with 17 or more years of relevant biopharma and/or regulatory experience including previous leadership experience; alternatively, a master's degree is preferred with 15 or more years of related experience, or a PhD with 12 or more years of related experience.
  • Demonstrated ability to influence across functions and organizational levels, build consensus, negotiate persuasively, and address disagreements constructively.
  • Ability to manage ambiguity and uncertainty in decision-making.
  • Experience leveraging relationships with other companies, trade associations, and government-industry coalitions to advance organizational interests.
  • Record of developing talent through informal mentorship and direct supervisory relationships.
  • Ability to cultivate a workforce through hiring, promotion, and staff development aligned with current and emerging talent needs.
  • Commitment to ethical professional behavior and creating a productive and respectful work environment.
  • Strong interpersonal, problem-solving, analytical, and organizational skills, with accountability.
  • Ability to ensure compliance with regulatory requirements.
  • Extensive experience developing regulatory strategy across early and commercial stages of development.
  • Experience supporting or maintaining commercial products, with understanding of lifecycle management and post-marketing regulatory strategy.
  • Ability to synthesize scientific, clinical, safety, and business inputs into cohesive regulatory strategy.
  • Strong presentation and communication skills to convey complex regulatory strategy to audiences with varying levels of sophistication.
  • Expertise in FDA regulatory frameworks and the evolving regulatory policy landscape.

Responsibilities

  • Lead development and execution of global regulatory strategies across early- and late-stage Endocrinology programs, including rare and obesity indications.
  • Integrate scientific, clinical, safety, and commercial considerations into regulatory roadmaps from first-in-human through post-marketing lifecycle management.
  • Provide guidance on complex regulatory issues to cross-functional teams and senior management, including the benefits and risks of different regulatory strategies.
  • Translate regulatory requirements into differentiated strategy and business opportunity.
  • Serve as a senior regulatory voice on safety signals, benefit-risk assessment, and strategic response planning.
  • Partner with Clinical Development, Safety, Commercial, CMC, Quality, and Legal to align regulatory strategies and support value creation.
  • Contribute to portfolio and commercial decisions as a strategic thought partner to senior leaders.
  • Present data-driven cases for strategic direction, negotiate persuasively, and address disagreements constructively to build consensus.
  • Coach teams in making timely, high-quality decisions that balance uncertainty with decisive action.
  • Lead and develop a team of three regulatory strategists, fostering accountability, growth, and high performance.
  • Develop talent through informal mentorship and direct supervisory relationships.
  • Hire, promote, and develop staff in alignment with current and emerging talent needs.
  • Champion ethical professional behavior and foster a productive, respectful, and inclusive work environment.
  • Ensure compliance with global regulatory requirements across assigned programs.
  • Guide teams in navigating regulatory ambiguity while maintaining integrity and compliance.
  • Contribute to broader regulatory leadership initiatives and enterprise governance forums as needed.

Desired Qualifications

  • A master's degree with 15 or more years of related experience is listed as preferred.
  • Deep understanding of regulatory strategy within rare disease and/or obesity markets is strongly preferred.
  • Experience across diverse therapeutic modalities, such as antibodies, peptides, and small molecules, is preferred.

About the Company

Neurocrine Biosciences

Develops and markets neurology-focused therapies

Neurocrine Biosciences develops and commercializes medicines for neurological and endocrine diseases. Its work centers on discovering and developing treatments, with INGREZZA (valbenazine) approved to treat adults with tardive dyskinesia and a pipeline of other drug candidates in various clinical stages. The company earns revenue from sales of approved medicines and from milestones and royalties from collaborations with partners. By focusing on both neurological and endocrine conditions, Neurocrine targets patients and healthcare professionals seeking therapies for conditions such as tardive dyskinesia, Parkinson's disease, and endometriosis. Its main goal is to bring therapies to market through development and commercialization, supported by ongoing research across its clinical programs to address unmet medical needs in these areas.

Company size
1,001-5,000
Company stage
IPO
Headquarters
San Diego, CA
Founded
1992

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