Senior Scientist, Non-Regulated Bioanalysis and PK Operations

Neurocrine Biosciences; San Diego (CA); Sur place; USD 110 000 - 150 000; Plein temps

Résumé du poste

Neurocrine Biosciences is seeking a Senior Scientist in Bioanalysis & PK Operations to oversee non-regulated studies, coordinating bioanalytical, PK and TK activities. The role focuses on planning and execution with external CROs, ensuring study quality and timely delivery.

Responsibilities include outsourcing management, data generation, and contributing to IND/CTA documentation, while collaborating across functional teams and data platforms.

Qualifications

• PhD in pharmaceutical sciences, pharmacokinetics, bioanalysis, biology or related field with 2+ years industry experience.
• MS with 4+ years industry experience.
• BS with 6+ years industry experience.
• Experience supporting nonclinical PK, pharmacology, toxicology studies.
• Knowledge of bioanalysis and PK workflows.
• Vendor management and study coordination skills.
• Familiarity with electronic data management platforms preferred.

Responsabilités

• Manage outsourcing of BA/PK/TK studies and CRO/vendor relationships.
• Coordinate reagent development logistics, sample and shipping operations, study documentation and cross-functional workflows.
• Contribute to study reports and IND/CTA documentation.

Connaissances

Vendor management

Study coordination

Nonclinical PK/pharmacology/toxicology

Bioanalysis workflows

Cross-functional collaboration

Formation

PhD in pharmaceutical sciences / pharmacokinetics / bioanalysis / biology

MS with 4+ years industry experience

BS with 6+ years industry experience

Description du poste

Role

Senior Scientist in Bioanalysis & PK Operations supporting non-regulated studies at Neurocrine Biosciences, focusing on planning, coordination, and execution of bioanalytical, PK, and TK activities.

Responsibilities

• manage outsourcing of BA/PK/TK studies, CRO/vendor relationships, reagent development logistics, sample and shipping operations, study documentation, and cross-functional workflows
• contribute to study reports and IND/CTA documentation

Requirements

• PhD in pharmaceutical sciences, pharmacokinetics, bioanalysis, biology, or related field with 2+ years
• MS with 4+ years
• BS with 6+ years industry experience
• experience supporting nonclinical PK, pharmacology, toxicology studies
• knowledge of bioanalysis and PK workflows
• vendor management and study coordination skills
• familiarity with electronic data management platforms preferred

High Value

• non-regulated bioanalysis, PK, TK, study outsourcing, CRO/vendor management, international sample logistics, IND/CTA documentation

Work Setup

not specified, but involves cross-functional collaboration; no travel specified.