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.
Intern, Quality Assurance
Neurocrine is seeking a part-time intern to assist with the QA function with Quality Systems implementation and maintenance.
Director, Regulatory Affairs
The Regulatory Director will influence organizational decisions that involve multiple groups and/or locations.
Sr. Medical Writer
The Medical Writer will participate as a member of the Regulatory Affairs/ Medical Writing group and is held accountable for accurate and timely completion of assigned documents.
Part-time Lab Assistant, Biology
Neurocrine seeks a highly motivated detail-oriented student intern to work within its Research division. The intern will receive expert training in applied life sciences within Neurocrine's state-of-the-art drug discovery laboratory.
Temporary HR Coordinator
This individual provides general Human Resources support including administration of company benefit programs, HRIS, New Hire Orientation, interview scheduling, maintenance of employee records, company events and special projects as needed.
Clinical Document Specialist
Under general guidance from the Director of Clinical Operations and the Clinical Trial Manager, the Document Specialist will support the clinical team in clinical document processing from study start up through archival of completed study.
Clinical Trials Assistant
Under general guidance from the Director of Clinical Operations and the Clinical Trial Manager, you will support the Clinical team responsible for management of multiple clinical trials (all phases), and assure compliance with GCP and ICH guidelines.
Principal Investigator, Analytical Development
The individual will independently support the NDA filing activities of Chemical Development related principally to the Neurocrine VMAT-2 program. The successful candidate will write CMC analytical sections of regulatory filing documents in CTD format based on data provided by collaborating CMOs.
Scientist, Chemical Development
The individual will independently conduct synthesis and process development activities for preclinical and clinical candidates. This includes laboratory experimentation for compound preparation, synthetic route scouting, process development/optimization, and process troubleshooting.
The Buyer will obtain materials and services from suppliers at the lowest cost consistent with considerations of quality, service, and company policy and procedure.
Marketing Analyst / Manager
This individual will be responsible for developing and maintaining market assessments and commercialization plans for our development programs, and build collaborations with Research and Development, and help to shape the pipeline to maximize commercial success.
Manager, Clinical QA
This individual will manage GCP QA activities in support of NBI development projects and commercial product clinical trials.