Summary

We are seeking a highly motivated and organized Scientist to support critical reagent activities across Research through Clinical development. The role will provide operational and onsite support for critical reagent inventory, logistics, documentation, and both internal and outsourced reagent-generation and characterization activities. The candidate will partner closely with the Critical Reagent Senior Scientist and cross-functional teams to ensure critical reagents are appropriately tracked, available when needed, and supported by accurate and current documentation. Success in this role will require strong organization and attention to detail, effective project coordination, comfort working across multiple electronic systems, and the ability to collaborate with internal teams and external CRO/CDMO partners.

Job description

About the Role

We are seeking a highly motivated and organized Scientist to support critical reagent activities across Research through Clinical development. The role will provide operational and onsite support for critical reagent inventory, logistics, documentation, and both internal and outsourced reagent-generation and characterization activities. The candidate will partner closely with the Critical Reagent Senior Scientist and cross-functional teams to ensure critical reagents are appropriately tracked, available when needed, and supported by accurate and current documentation. Success in this role will require strong organization and attention to detail, effective project coordination, comfort working across multiple electronic systems, and the ability to collaborate with internal teams and external CRO/CDMO partners.

Your Contributions (include, but are not limited to):

Coordinate receipt, storage, inventory, distribution, and shipment of critical reagents to internal teams and external partners
Monitor reagent inventory and supply levels, identify upcoming needs, and coordinate replenishment and resupply activities
Maintain accurate reagent records and inventory information across Smartsheet, Benchling, FreezerPro, and other applicable systems
Maintain and organize reagent characterization, qualification, CoA, inventory, and shipping documentation to support material traceability
Coordinate operational activities for outsourced critical reagent-generation campaigns, including timelines, deliverables, samples, shipments, documentation, and action items
Interface with CRO/CDMO partners on routine campaign activities and escalate scientific, quality, supply, or timeline issues as appropriate
Support SOWs, Change Orders, purchase orders, and procurement workflows and coordinate with internal functions and external vendors
Develop and maintain project trackers and support development of standardized workflows and processes to improve reagent availability, traceability, and operational readiness
Support defined reagent-generation activities and campaigns, including antibody and other critical reagent production activities
Prepare project, campaign, and inventory updates and maintain action-item and milestone tracking for recurring Critical Reagent meetings

Requirements

BS/BA in Biology, Biochemistry, Chemistry, Pharmaceutical Sciences, or related scientific field with 4+ years of relevant biotechnology or pharmaceutical industry experience OR
MS/MA with 2+ years relevant industry experience OR
PhD and some relevant industry experience
Experience supporting scientific operations, bioanalytical activities, reagent management, laboratory operations, or related drug-development activities
Strong organizational and project coordination skills with the ability to manage multiple activities, timelines, and priorities
Experience with scientific inventory, data-management, or project-tracking systems; experience with Smartsheet, Benchling, and/or FreezerPro is preferred
Familiarity with antibodies, bioanalytical reagents, or critical reagent development and lifecycle activities is preferred
Experience working with external CROs/CDMOs or scientific vendors is preferred
Strong attention to detail with demonstrated ability to maintain accurate and traceable scientific documentation
Strong written and verbal communication skills and ability to work independently and collaboratively in a cross-functional team environment

Benefits

401(k) Matching
Paid Vacation
Paid Holidays
Personal Days
Paid Caregiver Leave
Paid Parental Leave
Paid Medical Leave
Medical, Dental & Vision
Annual Bonus
Equity Incentive Program

Company overview

Neurocrine Biosciences is a leading neuroscience-focused biopharmaceutical company founded in 1992 and headquartered in San Diego, California. The company specializes in discovering and developing life-changing treatments for patients with under-addressed neurological, neuroendocrine, and neuropsychiatric disorders. Neurocrine's diverse portfolio includes FDA-approved treatments for tardive dyskinesia, chorea associated with Huntington's disease, classic congenital adrenal hyperplasia, endometriosis, and uterine fibroids. Their flagship product, INGREZZA (valbenazine), was the first FDA-approved treatment for adults with tardive dyskinesia. The company maintains a robust pipeline with multiple compounds in mid- to late-phase clinical development across core therapeutic areas, including Parkinson's disease, Tourette syndrome, and major depressive disorder. Neurocrine operates with a purpose to relieve suffering for people with great needs, applying unique insights into neuroscience and the interconnections between brain and body systems to treat complex conditions. The company is publicly traded on NASDAQ under the symbol NBIX and has established strategic collaborations with major pharmaceutical partners including AbbVie.