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.

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:

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• Coordinate, align, and monitor research and development activities for program-specific cross-functional plans and risks

• Coordinates project timelines to support R&D goals from both a technical and business operations perspective

• Supports outsourced development and clinical/commercial manufacturing activities, as it relates to business, contract, financial management, and/or operational efficiencies

• Manages the operational activities (schedule, timelines, cost) of the vendors, ensuring cost, quality, metrics, delivery and program objectives are met. Manages operational risk at the vendors

• Assists in CDMO site evaluation/selection, preparation of the request for proposal (RfP) and contracting process

• Partners with key stakeholders in the preparation and negotiation of RFQs, RFPs, Statements of Work (SOW), and Supply Agreements; provides guidance on drafting documents and works with legal to ensure documents are processed in a timely manner

• Serve as a program point-of-contact within R&D

• Facilitate communications between key science and management stakeholders, as needed

• Collaborates with multiple functional lines (R&D, Regulatory, Quality Assurance, Clinical, Legal, Finance) within the company

• Facilitates and schedules meetings with internal personnel, as needed, to ensure cross-functional participation on the project teams

• Collaborates with (may lead) internal cross-functional teams and vendors to determine development, clinical, and commercial manufacturing requirements, identify and mitigate key risks, and ensure that plans are executed as intended

• Proactively identifies and champions new process and/or improvements, and solutions to complex issues at the vendors

• Anticipates stakeholder needs and provides visibility to key stakeholders on all vendor matters, tactical & strategic, and manages stakeholder priorities across all Neurocrine activities at the vendors

• Partners with Neurocrine Quality Assurance to ensure vendors are in compliance with all cGLP/cGMP guidelines and Neurocrine SOP requirements

• Tracks spend and plans resource allocation at contract vendors

• Supports in providing monthly/quarterly accruals to Accounting/Finance

• Supports in high-level management of department's annual budgeting process

• Supports in high-level management of department's CapEx spend on equipment purchase

• Other duties as assigned

• BS/BA degree in Chemistry, Biochemistry or related discipline and 5+ years of Pharmaceutical industry experience. Hands-on experience executing and interpreting pharmaceutical analysis, and drug product unit operation processing is preferred OR

• MS/MA degree in Chemistry, Biochemistry or related discipline preferred and 3+ years of similar experience as noted above OR

• PhD in Chemistry, Biochemistry or related discipline and some relevant experience; may include postdoc experience OR

• Demonstrates solid level of understanding project / group goals and methods

• Consistently recognizes anomalous and inconsistent results and interprets experimental outcomes

• Able to explain the process behind the data and implications of the results

• Strong knowledge of one or more scientific disciplines, becoming expert in one discipline.

• Strong knowledge of scientific principles, methods and techniques

• Strong knowledge and demonstrated ability working with a variety of laboratory equipment/tools

• Ability to work as part of a team; may train lower levels

• Excellent computer skills

• Strong communications, problem-solving, analytical thinking skills

• Detail oriented yet can see broader picture of scientific impact on team

• Ability to meet multiple deadlines, with a high degree of accuracy and efficiency

• Strong project management skills

• Strong understanding of cGLPs and cGMPs relating to pharmaceuticals

• Must be self-motivated, detail-oriented, possess familiarity of physical & analytical techniques as they pertain to biopharmaceutical properties

• Ability to learn quickly and think independently

• Exhibit strong scientific acumen

• Demonstrated understanding of chemical and instrumental methods for analyses of development compounds, drug substances, raw materials, intermediates, drug products, and packaging materials.

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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.

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