Senior Pharmaceutical Toxicology Consultant

BlueRidge Life Sciences; California; On-site; USD 180,000 - 280,000; Full time

Job summary

BlueRidge Life Sciences is seeking an experienced toxicologist to lead nonclinical safety programs for pharmaceutical clients in California. The role involves designing, overseeing, and interpreting toxicology studies and aligning with ICH/regulatory guidelines.

Collaborate with epidemiologists, engineers, and biostatisticians to support regulatory submissions and interactions with agencies. Ph.D. in toxicology or related field and 15+ years pharma experience are preferred.

Qualifications

• Ph.D. in toxicology, pharmacology, or related sciences.
• Minimum 15+ years of pharmaceutical consulting or industry experience.
• Familiarity with ICH guidelines and regulatory agency processes.

Responsibilities

• Oversee nonclinical safety programs across drug development stages.
• Interpret safety data and integrate TK/PK/PK-PD findings.
• Prepare regulatory submission sections and liaise with agencies.
• Lead project teams and manage multiple high-priority programs.

Skills

Project management

Written communication

Verbal communication

Education

Ph.D. in toxicology or related sciences

Job description

BlueRidge Life Sciences is seeking an experienced toxicologist to lead nonclinical safety programs for pharmaceutical clients in California. The role involves designing, overseeing, and interpreting toxicology studies and aligning with ICH/regulatory guidelines.

Collaborate with epidemiologists, engineers, and biostatisticians to support regulatory submissions and interactions with agencies. Ph.D. in toxicology or related field and 15+ years pharma experience are preferred.