Senior Toxicology Consultant – Pharma

BlueRidge Life Sciences; Juneau (AK); On-site; USD 180,000 - 240,000; Full time

Job summary

BlueRidge Life Sciences is seeking a highly experienced toxicologist to join its ToxStrategies division. The role focuses on guiding nonclinical safety assessments for biopharmaceutical programs, designing studies, and interpreting data across development stages, including interactions with regulatory authorities.

Ideal candidates have a Ph.D. in toxicology or related field with 15+ years in pharma/consulting, and a strong track record in regulatory documentation and cross-functional teams.

Qualifications

• Ph.D. required in toxicology, pharmacology, or related sciences.
• Minimum 15+ years in biopharmaceuticals, consulting, or industry.
• Familiar with ICH and regulatory guidance for nonclinical development.
• Experience writing regulatory documents and interacting with authorities.
• Experience overseeing nonclinical safety programs across development phases.
• Strong project management and leadership skills.

Responsibilities

• Oversee nonclinical safety programs across all development phases.
• Lead study design, data interpretation, and safety assessments.
• Serve as toxicology representative on project teams and with regulators.
• Prepare regulatory documents and interact with agencies (FDA, EMA).
• Contribute to business development and client proposals.
• Travel may be required (up to ~20%).

Skills

Project management

Written communication

Verbal communication

Independence

Team collaboration

Regulatory knowledge

Data interpretation

Education

Ph.D. in toxicology or related sciences

DABT certification (desired)

Job description

BlueRidge Life Sciences is seeking a highly experienced toxicologist to join its ToxStrategies division. The role focuses on guiding nonclinical safety assessments for biopharmaceutical programs, designing studies, and interpreting data across development stages, including interactions with regulatory authorities.

Ideal candidates have a Ph.D. in toxicology or related field with 15+ years in pharma/consulting, and a strong track record in regulatory documentation and cross-functional teams.