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.
Click here to apply to any of the careers listed below.
This is a temp to hire position. Responsible for day to day facilities operations to include:
• General building repair & maintenance
• Installation, repair, and maintenance of furniture/fixtures/equipment in both lab and office areas
• Special projects as assigned to support both the facilities and EHS teams
Manager, Regulatory Affairs
SUMMARY: Manages the day to day CMC regulatory activities for one or more development and/or marketed projects and through this is responsible for achieving results that impact the success of the department and company.
Manager / Senior Manager, Packaging Operations
SUMMARY: The Manager / Senior Manager, Packaging Operations will ensure that marketed products are packaged into finished goods in a reliable, compliant, cost-effective and timely fashion to meet commercial demand. This role manages the relationships, contracts, and activities of assigned commercial contract packagers within the Neurocrine supply chain network.
The Associate/Project Manager will support one or more product development teams to drive team performance and communication. You will ensure that cross-functional teams are aligned on goals and timelines and work with them to deliver milestones on or ahead of schedule. You will escalate issues that require management review as well as highlight team successes to the wider organization.
Supports attorneys and paralegals in implementing, managing and improving the company’s Contracts Management System Lifecycle Process.
ESSENTIAL DUTIES AND RESPONSIBILITIES
• Manages the contract review and approval process and tracks department metrics
• Manages the company’s contract management system and acts as the primary contact at the company for the contact management system
Sr. Clinical Database Specialist
The Senior Clinical Database Specialist is responsible for independently performing data management tasks, including clinical study database design and build, as well as providing oversight and leadership to support both in-house and outsourced clinical trials.
Sr. Clinical Data Management Associate
This position is responsible for independently performing data management tasks and providing oversight and leadership to support the development, design, implementation, and validation of clinical study databases for both in-house and outsourced clinical trials for all clinical studies/programs
Head of Sales Operations
This position will lead the team responsible for sales operations functions in support of the Company’s sales force and national accounts staff, and certain functions for the Medical Scientific Liaison (MSL) team. The individual will ensure processes, systems and tools are in place to support sales productivity and effectiveness, targeting/alignment, sales force automation/customer relationship management (SFA/CRM), sample management, incentive compensation (IC), field reporting, etc.
Postdoctoral Fellow, Chemistry
Highly motivated Postdoctoral Fellow wanted to play a key role in applying modern synthetic chemistry to synthesize novel chiral building blocks, conduct innovative publishable science, scouting and hands-on experience with both micro- and maco-scale reactions as well as automated synthesis and purification. The fellow will synthesize valuable intermediates amenable for automated synthesis over a two-year period.
Medical Communications Specialist
The Medical Communications Specialist reports to the Director, Medical Communications and will be a key contributor to the Medical Communications team to develop key initiatives that are instrumental for the organization. Responsibilities will include coordinating publications, building and managing library services and completing other medical affairs projects as assigned.
Sr. Talent Acquisition Specialist
As a key team member of our growing HR team, the Sr. Talent Acquisition Specialist will identify, source, assess and hire a variety of positions within Neurocrine Biosciences. This position works closely with our HR business partners to create a positive candidate experience, act as a valuable resource, and collaborate seamlessly across multiple client groups. May also include recruiting responsibilities such as coordinate and schedule interviews, assist with streamlining processes and other duties as assigned.
Regulatory Affairs Specialist
ESSENTIAL DUTIES AND RESPONSIBILITIES include, but are not limited to:
• Assists with the preparation of submissions to regulatory authorities, with minimal supervision (e.g. clinical trial applications, initial IND and maintenance submissions, annual reports, expedited safety reports).
• Performs quality checks of regulatory submission documentation and electronic publishing output.
• Conducts review of clinical regulatory documents.
Scientist, Discovery Bioanalytical
The Scientist, Discovery Bioanalytical responsibilities will include providing technical expertise, conducting laboratory experiments with hands-on LC/MS/MS method development, and multi-project management.
QC Data Review Specialist
The QC Data Review Specialist will be responsible for assisting in the oversight of laboratory analyses and operations as they relate to QA. This key functional role will operate within a cross-functional GXP QA Team and supports internal QA functions. This position will be responsible for reviewing and maintaining cGMP analytical documentation, interacting with manufacturing vendors and analytical contract labs and assist in the conduct of external and internal audits. The QA Specialist shall provide oversight to ensure compliance with company policies and procedures, ICH, FDA and EU requirements, cGMP, and other applicable requirements.
Manager of Document Control
The Manager/Sr. Manager of Document Control will oversee documents (both electronic and paper copies) within Quality Assurance, Regulatory Affairs, and other key departments at Neurocrine to ensure that all GXP regulated documents are filed systematically and are easily retrievable. Duties will include management of GXP records, lifecycle management of records, maintenance of the document database, and troubleshooting document issues and requests.
Principal Investigator, Research (Biology)
Primary role will be to work closely with the group to identify new drug target opportunities and expand our drug pipeline, through in-house research studies, the establishment of external collaborations, and the application of new technologies. The successful applicant will have a rich knowledge of neuroscience, endocrinology, and cell and molecular biology, and can apply their experience to drug target identification and validation.
Principal Investigator, Toxicology
The Principal Investigator will have a key role in the discovery and development of Neurocrine’s development compounds. Working with Neurocrine colleagues, the Principal Investigator will participate in all stages Toxicology/Safety Pharmacology assessment, from study planning through to regulatory submission. In this role, the individual will provide strategic and operations direction ensuring all studies are conducted in line with appropriate guidelines and regulatory testing standards and individual program objectives. The individual will also represent Toxicology on Development teams and regularly interface with colleagues to ensure timely and accurate dissemination of Toxicology/Safety pharmacology findings.
Manager, Medical Affairs, Training & Operations
This position will be responsible for the overall Medical Affairs needs in training, metrics, planning and operations. The position will work closely with Medical Science Liaison (MSL), Health Economics and Outcomes Research (HEOR), and Medical Communications leadership to develop the on-boarding and training curriculum for Medical Affairs staff, strategic business plans and goals, annual budgets, reporting metrics, information system requirements and associated reporting capabilities. In addition, the position will report to the Head of Medical Affairs and be a member of the Medical Affairs senior leadership team.
Manager, Medical Communications
The Medical Communications Manager will be a key contributor within the Medical Communications Department and serve as an expert scientific content resource for the broader organization with a diverse set of responsibilities.
As Scientist, Preformulation, the employee will design and execute preformulation and physical characterization studies to support product development from early discovery through commercialization. Fully characterize API and Drug Product (DP) materials to inform development decisions for Research, Preformulation, Chemistry, and Formulation.
Scientist – Tissue Culture
The primary role will be to provide tissue culture support for multiple drug discovery programs by managing multiple cell lines per the stage of the program.
ESSENTIAL DUTIES AND RESPONSIBILITIES (include, but are not limited to):
Responsibility for cell culture maintenance, reagent preparation, cell plating for use in assays, cell line generation, culture expansion, cryopreservation, and membrane preparation.
Principal Investigator, Analytical
The Analytical Development Principal Investigator will report directly to the Sr. Director of Analytical Development and lead the progression CMC analytical activities for one or more of Neurocrine’s pipeline projects.
Assist Chief Financial Officer by performing Treasury functions, risk management analysis, tax compliance, revenue analysis, forecasting and managing financial administration.
Principal Investigator, Chemical Development
Responsible for research and development, tech transfer and commercialization of drug substance processes, as well as oversight of batch manufacturing and regulatory document contribution through managerial and individual input. Provides project management for Chemical Development projects.
The Scientist, Formulation Development will be responsible for supporting formulation of solid oral drug products to support clinical development though registration and initial commercialization. The primary functions encompass product development and manufacturing with secondary functions supporting the other pharmaceutical sciences departments as required.
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.
MEDICAL DIRECTOR (DRUG SAFETY AND PHARMACOVIGILANCE)
The Medical Director (Drug Safety Physician) is accountable for comprehensive review and analysis of safety information. This position is responsible for performing safety case report review and other pharmacovigilance related activities in accordance with FDA regulations, ICH guidelines and applicable SOPs. In collaboration with the other departments, ensures effective management and communication of the benefit/risk profile of the product. Neurocrine has a smaller, entrepreneurial environment, and offers the opportunity to have broader involvement in many activities.
Head of Investor Relations
Reporting to the President & Chief Operating Officer, the Head of Investor Relations 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.