Senior Regulatory Strategy Manager

Neurocrine Biosciences, Inc.; San Diego (CA); On-site; USD 180,000 - 210,000; Full time

Job summary

Neurocrine Biosciences, Inc. is seeking an experienced Regulatory Affairs professional to provide project leadership for regulatory submissions and process improvements.

You will work with regulatory leadership to prepare submissions, maintain processes, and ensure compliance with global requirements. The role involves coordinating with internal departments and external partners to drive early approvals of clinical trial applications and labeling decisions while staying aligned with company

Qualifications

• BS/BA in Life/Health Sciences with 8+ years in regulatory affairs in drug development.
• Experience with FDA regulations and ICH guidelines for regulatory submissions.
• Leadership experience: minimum 2 years in a lead capacity.

Responsibilities

• Provide project leadership to develop, review and file INDs, CTAs and regulatory documents such as DSURs.
• Collaborate on global regulatory strategies with cross-functional teams (CMC, nonclinical, clinical).
• Develop and manage regulatory submission timelines and documents.
• Mentor or train less experienced colleagues to share best practices.
• Interface with US and international regulatory authorities as required.
• Lead or contribute to regulatory filing document reviews and strategy.

Skills

Regulatory affairs

FDA regulations

ICH guidelines

Education

BS/BA in Life/Health Sciences

Master's in Life/Health Sciences preferred

Job description

Who We Are:

Neurocrine Biosciences is a leading biopharmaceutical company with a simple purpose: to relieve suffering for people with great needs. We are dedicated to discovering, developing and commercializing life-changing treatments for patients with under-addressed neurological, psychiatric, endocrine and immunological disorders. The company's diverse portfolio includes FDA-approved treatments for tardive dyskinesia, chorea associated with Huntington's disease, classic congenital adrenal hyperplasia, hyperphagia in Prader-Willi syndrome, 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 more than 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 , Facebook and YouTube . ( *in collaboration with AbbVie )

About the Role:

Provides project leadership support for the overall regulatory department with process development/improvement activities to support organizational optimization and more consistent and seamless interaction with internal and external stakeholders. Works closely with all Regulatory depts. as well as cross-functionally and with external partners and CRO's. Will Work closely with the Regulatory leadership to prepare regulatory submissions (authoring, timeline planning, etc.). Develops and maintains department regulatory processes. Performs the coordination and preparation of document packages for regulatory submissions for new and mature products to ensure alignment and compliance with local and regional registration requirements as well as with company policies from all areas of company as well as internal audits and inspections. Compiles all materials required in submissions, license renewal and annual registrations. Takes the lead to recommend and implement changes for labeling, manufacturing, marketing and clinical protocol for regulatory compliance. Monitors and improves tracking/control systems. Keeps abreast of regulatory procedures and changes. May have direct interaction with regulatory agencies on defined matters. Recommends strategies for earliest possible approvals of clinical trials applications.

Your Contributions (include, but are not limited to):

• Provide project leadership to develop, review and/or file INDs, CTAs, briefing documents and maintenance of development and approved applications including authoring DSURs, annual reports, amendments as needed
• Provide regulatory representation and expertise on cross-functional product development teams as needed. Collaboratively develop global regulatory strategies to support CMC, nonclinical, and clinical activities across various development programs
• Maintain an awareness, through regulatory intelligence, of global regulatory strategies for products in the same class/indication and determine applicability to Company programs
• Develop and manage project timelines for regulatory submissions.
• Lead, coordinate, author, critically review and provide strategic input on regulatory filing documents
• Lead the regulatory review of clinical study documentation, including review of clinical protocols, informed consent documents, and clinical study recruitment materials
• Conduct regulatory research and analysis, develop and communicate recommendations regarding new/emerging regulations to management and project teams
• Develop and implement standard operating procedures and department working practices
• Ensures the company is adhering to all applicable government regulations
• Interface directly with US and international regulatory authorities on specific projects when required
• Lead or partner with team members to complete assigned activities with the project team
• Mentor or train less experienced colleagues to provide an example of innovation and excellence
• Contribute to the development of strategic Regulatory plans and processes
• Other duties as assigned

Requirements:

• BS/BA degree in Life/Health Sciences AND 8+ years of progressive industry experience of which a minimum of 6 years must be Regulatory Affairs experience in drug development at a research-based pharmaceutical company, including two years in a lead capacity. Experience with FDA regulations and ICH guidelines for regulatory submissions. OR
• Master's degree in Life/Health Sciences preferred AND 6+ years of related experience
• Anticipates business and industry issues; recommends relevant process improvements
• Demonstrates broad expertise or unique knowledge
• Considered an expert within the company and may have external presence in area of expertise
• Applies in-depth expertise in discipline and broad knowledge of other closely related areas to improve efficiency