Non-Clinical Senior Toxicologist

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

$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.
Strong motivation, independence, and the ability to work in a fast-paced, multidisciplinary, matrix environment with minimal supe
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