Jobs

Non-Clinical Senior Toxicologist

• Foster City, CA
• Direct Hire
• Job ID: BN38-2690678

Salary Range: $1 to $2 Per Year

SENIOR PROJECT TOXICOLOGIST Sr. Research Scientist II, Non Clinical Safety and Pathobiology 

Associate Director and also Director level available

Key Aspects:

The Sr. Project Toxicologist works in a project team-based research structure to lead and collaborate with new and ongoing projects. 

Serves as a nonclinical safety development resource, working with other members of the department regarding strategy for nonclinical safety programs.

• Plays key role on cross functional teams – both Research and Development Project Teams where he/she is responsible for design, implementation, oversight and analysis of nonclinical programs to support drug development candidates across a variety of platforms.
• Writes and reviews regulatory documents to support global regulatory filings.
• Manages multiple projects simultaneously with minimal supervision.
• Reviews protocols, data and study reports ensuring presentation of data in report is accurate and supports the conclusions.
• Interprets and puts data into context with literature and project goals.
• Provides independent technical contributions.
• Actively supports the integration of early nonclinical safety strategies throughout Research.
• Potential to lead Non-Clinical Development sub-teams.
• Solves complex problems requiring thorough scientific assessment.
• Models behaviors that nurture a culture of innovation.
• May participate in and lead significant process improvement initiatives that may impact the department.
• Communicates effectively cross-functionally to accomplish company goals.
• Be a team player who thrives in a high speed environment where autonomy, accountability and innovation are critical for success.
• Strong knowledge and scientific expertise in subject area/discipline; familiar with other disciplines inside and/or outside of department
• Knowledge of nonclinical requirements to support research projects.
• Knowledge and understanding of GLPs.
• Knowledgeable of regulatory requirements, including ICH requirements and other regional requirements.
• Possesses a basic understanding of guidance that impacts drug development.
• Is sought out for advice by others within the department and related functional areas.
• PhD in Toxicology or a related scientific discipline with 8+ years of biopharmaceutical or CRO industry
• Board certification is desirable.
• Demonstrable innovative, flexible and critical thinking skills and experience applied to hypothesis-driven nonclinical safety research.