Study Director III - Toxicology (Nonclinical GLP)

Labcorp

Madison (WI)

Sur place

USD 110 000 - 140 000

Plein temps

Il y a 9 jours
Générateur de candidature

Une candidature conçue pour ce poste — un CV et une lettre de motivation personnalisés qui correspondent à l’offre.

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Avantages offerts par ce poste

Relocation assistance
401(k) plan
Tuition Reimbursement

Résumé du poste

Labcorp in Madison, WI is seeking a Study Director III - Toxicology to lead nonclinical toxicology studies, representing the single point of control and ensuring GLP compliance. You will interpret data, document results, and maintain regulatory alignment while serving as the primary client liaison.

Preferred candidates hold a PhD in toxicology or related fields and have CRO or pharma non-clinical development experience, with strong communication and project-management skills.

Qualifications

  • Master’s degree in toxicology, biology, chemistry, biochemistry, or molecular biology with 3+ years of research experience.
  • PhD in toxicology or related fields preferred.
  • Experience at a Contract Research Organization (CRO) or pharmaceutical non-clinical drug development is valued.
  • Strong client relationship and communication skills are expected.

Responsabilités

  • Serves as a Study Director, Principal Investigator, or Contributing Scientist for nonclinical toxicology studies under GLPs.
  • Represents the single point of control for safety assessment studies and bears legal responsibility for the study.
  • Main client contact and advisor for ongoing studies, understanding Sponsor requirements.

Formation

Master's degree in toxicology or related field
PhD in toxicology, regenerative biology, genetics, virology, or immunology

Description du poste

Labcorp in Madison, WI is seeking a Study Director III - Toxicology to lead nonclinical toxicology studies, representing the single point of control and ensuring GLP compliance. You will interpret data, document results, and maintain regulatory alignment while serving as the primary client liaison.

Preferred candidates hold a PhD in toxicology or related fields and have CRO or pharma non-clinical development experience, with strong communication and project-management skills.

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