The Sr. Scientist will develop assays for peptide and protein therapeutics, optimize formulations, and manage preclinical studies and collaborations.

The role involves strategic planning and execution of drug product development for clinical programs, including formulation and manufacturing processes for biologics, while managing relationships with external parties.

Design and develop drug formulations for peptide and protein delivery, manage CDMO partners, and support clinical studies with analytical methods.

The IT Business Partner will oversee technology strategies for Accounting, Finance, and Supply Chain, ensuring effective project management and compliance with regulations.

The Scientist will design, develop, and execute biological methods for gene therapy and biologic assets, collaborating with cross-functional teams to ensure quality and potency through rigorous analysis and documentation.

The Senior Scientist will establish cell line development capabilities, create stable CHO cell lines, optimize production processes, and maintain documentation for regulatory support.

The Brand Marketing Intern will support marketing activities, collaborate with cross-functional teams, and complete a special project for Neurocrine Biosciences.

Leads statistical input for clinical studies, oversees biostatistics team, and ensures adherence to statistical standards in clinical development.

Lead design and management of Identity and Access Management solutions, implementing IAM automation and ensuring compliance in a life-sciences environment.

The Neurology Account Specialist is responsible for promoting Neurocrine products, developing relationships with healthcare professionals, and achieving sales targets.

Lead the DMPK team applying ADME science to enhance portfolio, design studies, mentor staff, and contribute to regulatory submissions.

As an analytical project leader, you will develop and validate analytical methods for drug products, oversee testing, and ensure compliance with regulatory requirements while managing project activities in a cGMP environment.

The Director of Government Affairs leads public advocacy efforts at Neurocrine Biosciences, focusing on federal and state legislative issues. The role involves strategic collaboration with internal stakeholders, managing lobbying operations, representing the company before officials, and ensuring compliance with regulations. Responsibilities include preparing legislative analysis, developing policies, and influencing public policy to align with corporate objectives.

Lead the operational setup and management of biomarker specimens in clinical trials, collaborating with teams to implement and execute biomarker strategies.

Responsible for managing IT application systems for Research and Early Discovery, providing technical support, and aligning technology solutions with business needs. Oversees projects, vendor relationships, and process improvements, ensuring compliance and effective communication across departments.

The Sr. Corporate Counsel will provide legal advice and risk guidance across various departments, draft and negotiate contracts, ensure compliance with government regulations, and manage outside counsel. This role requires expertise in corporate matters and the ability to collaborate with diverse stakeholders.

Develop and maintain data platforms and services, focusing on scalability, security, and performance while collaborating with cross-functional teams. Lead design and implementation while mentoring junior engineers.

Lead analytical development for antibodies and bio-conjugates, ensuring compliance with cGMP, and managing cross-functional team deliverables.

Responsible for coordinating R&D business operations, including project planning, vendor management, compliance, and financial oversight in the pharmaceutical industry.

As a Sr. Analyst, Business Systems, leverage NetSuite and Coupa to optimize finance, accounting, and procurement processes, ensuring system adoption and process improvements.