Senior Pharmaceutical Toxicology Consultant

BlueRidge Life Sciences; Manchester (NH); Presencial; USD 180.000 - 240.000; Jornada completa

Descripción de la vacante

BlueRidge Life Sciences is seeking an experienced toxicologist (15+ years) to join our Pharmaceutical toxicology consulting practice. You will design and oversee nonclinical safety programs, provide regulatory and scientific guidance, and interact with agencies like FDA/EMA.

You will collaborate with epidemiologists, engineers, and biostatisticians to deliver science-driven solutions, lead study design, and contribute to regulatory documents while supporting business growth.

Formación

• Ph.D. in toxicology, pharmacology, or related sciences; DABT certification is desired but not required.
• 15+ years of pharmaceutical consulting and/or pharmaceutical industry experience (or gov/ CRO).
• Deep knowledge of ICH and regulatory guidance for nonclinical development; experience with cross-functional drug development teams.

Responsabilidades

• Oversee nonclinical safety programs across all development phases (pre-IND to NDA/BLA).
• Write or supervise pharmacology/toxicology sections of regulatory submissions and investigator brochures.
• Interact with global regulatory agencies (FDA, MHRA, EMA) and manage study design, data interpretation, and reporting.
• Contribute to business development, client meetings, and strategy discussions; travel up to ~20%.

Conocimientos

Project management

Communication skills

Team collaboration

Regulatory interaction

Leadership potential

Educación

Ph.D. in toxicology

DABT certification

Descripción del empleo

BlueRidge Life Sciences is seeking an experienced toxicologist (15+ years) to join our Pharmaceutical toxicology consulting practice. You will design and oversee nonclinical safety programs, provide regulatory and scientific guidance, and interact with agencies like FDA/EMA.

You will collaborate with epidemiologists, engineers, and biostatisticians to deliver science-driven solutions, lead study design, and contribute to regulatory documents while supporting business growth.