At Neurocrine Biosciences, Inc. highly-motivated individuals are working as a team to make a significant impact upon our business while progressing in their careers. We believe we have the best environment for “sky-is-the-limit” creativity, contribution, and learning. Neurocrine’s people, science, and culture are the ingredients that will bring us success in our mission.
Notice to Search Firms/Third Party Recruitment Agencies (Recruiters)
The Human Resources team manages the recruitment and employment process for Neurocrine. To protect the interest of all parties involved, Neurocrine will only accept resumes from a recruiter if an executed search agreement is in place at the start of the recruitment effort. Unsolicited resumes sent to Neurocrine from recruiters do not constitute any type of relationship between the recruiter and Neurocrine and do not obligate Neurocrine to pay fees should we hire from those resumes. Recruiters are requested not to contact or present candidates directly to our hiring managers or employees.
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Facilities Specialist, Operations
Responsible for the day to day operations, repair & maintenance, and services for a 150K sf research and development lab facility. The successful candidate will have experience working within the biotech industry supporting building systems, supervising vendors and their related services, as well as conducting general facilities tasks.
The Bioanalytical Manager is responsible for overseeing the development and implementation of both internal and external bioanalytical methods in support of discovery, GLP toxicokinetic (TK) and clinical pharmacokinetic/pharmacodynamic (PK/PD) studies.
Assoc. Dir./Director, Clinical Pharmacometrics
This individual will be responsible for all internal and external clinical PK and PK/PD modeling and simulation activities. The primary initial responsibility will be to oversee the design, conduct, and reporting of modeling and simulation analyses conducted by external CROs in support of product registration of a small molecule therapeutic.
Stock Option Administrator
SUMMARY: This position is responsible for assisting with all aspects of Ironwood’s stock plan administration including stock options, restricted stock units and performance based restricted stock units. This position is an integral member of the Finance & Accounting team and will also support the financial monthly close.
Will primarily function in the role of a Medical Safety Physician with the Pharmacovigilance and Drug Safety Department and also function as a Medical Director in the clinical development programs. Neurocrine has a smaller, entrepreneurial environment, and offers the opportunity to have broader involvement in many activities.
The Executive Assistant works with general guidance and assumes responsibility for a definable portion of projects, administrative work and/or process primarily supporting the President & COO, and as needed, other executives of the company.
HRIS / Comp Analyst
The HRIS/Compensation Analyst partners with HR leaders on compensation philosophies, programs, policies and practices. Provides information and tools to effectively meet human capital and financial objectives for the organization and to ensure internal equity, external competiveness, and compliance with applicable laws, regulations and organizational policies.
Manager, Quality Assurance
An excellent opportunity for a permanent hire Clinical QA Manager needed for a dynamic growing pharmaceutical company based in San Diego working with both development and commercial products. Will be responsible for Clinical Quality Assurance (CQA) in support of research projects across multiple therapeutic areas. Additionally, the successful candidate will assist with providing QA support and training to ensure adherence with applicable regulatory requirements and company policies/procedures.
Director, Medical Communications
The Director of Medical Communications is responsible for providing leadership and direction for Medical Information, Publications, and other Scientific Communications, ensuring all department responsibilities, including the provision of accurate, timely and appropriate responses to inquiries from healthcare professionals, consumers and internal departments, are met in a manner consistent with corporate directives and regulatory guidelines.
Environmental Health and Safety/Operations Associate
Provides support for and monitors compliance of corporate environmental health and safety programs. Performs detailed and routine Operations tasks effectively and efficiently.
Manager, Formulation Development
The Manager, Formulation Development will be responsible for formulation development and clinical manufacturing of drug products for drug candidates to support preclinical studies, clinical development, registration and initial commercialization. The primary functions encompass product development and manufacturing with secondary functions supporting the other pharmaceutical sciences departments as required.
Sr. Clinical Data Management Associate
The Senior Clinical Data Associate (CDA) is responsible for independently performing data management tasks and providing oversight and leadership to support the development, design, implementation, and validation of in-house and outsourced clinical trials for all clinical studies/programs.
Associate Director, Commercial Analytics
This position supports marketing and product development strategic and tactical decision making for the Company as leader of the team responsible for providing objective, in-depth information and insights based on primary market research, secondary analytics, and advanced analytics.
1. Prepare dose formulations and other reagents as instructed.
2. Perform tissue collection and necropsies.
3. Collect, analyse, communicate results, and assist in preparing reports in a timely manner.
4. Work collaboratively with other scientists, technicians and colleagues as part of multidisciplinary project teams.
Clinical Operations Associate
Under general guidance, provide support to the clinical team in all aspects of clinical trial operations
Medical Science Liaison (OH, MI, IN, KY)
The Medical Science Liaison (MSL) organization is part of Medical Affairs within the Clinical organization. The MSLs will interact with scientific leaders and healthcare decision makers to communicate and advance the scientific platform for therapeutic areas that are aligned with the overall corporate strategy.
Vice President, Investor Relations and Corporate Communications
Reporting to the President & Chief Operating Officer, the Vice President of Investor Relations and Corporate Communications holds enterprise-level responsibility for strategic and tactical leadership of company communications. This broad role’s ultimate mandate is to ensure consistent messaging across all platforms to all stakeholders, both internal and external.
Senior Director, Strategic Marketing
SUMMARY: Reporting to the Chief Commercial Officer, this individual will direct early commercial planning and market research for Neurocrine's therapeutic candidates in phase III and earlier stage clinical development. This position is responsible for developing market opportunity assessments for current and potential pipeline programs including disease area understanding, competitive landscapes, unmet medical need, reimbursement environment and overall commercial attractiveness.
Principal Statistical Programmer
The Principal Statistical Programmer will play a lead role in supporting the statistical analysis and reporting of data from clinical and nonclinical studies.
Scientist – In Vitro
Seeking an individual with in vitro high-throughput screening and lead optimization experience, with proven assay optimization and assay automation skills. This individual will be an integral member of the pharmacology team supporting multiple new target screening and lead optimization campaigns.