Scientist, Nonclinical Safety

Role Summary

We are seeking a bright and enthusiastic Research Scientist to complement our Nonclinical Safety and Pathobiology group. The role serves as the toxicology representative on multifunctional project teams, owning the nonclinical safety program and contributing to regulatory documents to support drug development candidates across platforms from early research through registration/post approval. This is a site-based role in Foster City, CA at our global headquarters.

Responsibilities

• Manage multiple projects simultaneously with minimal supervision.
• Provide critical review and interpretation of protocols, data and study reports.
• Actively support the integration of early nonclinical safety strategies throughout Research.
• Solve moderately complex problems requiring thorough scientific assessment.
• Effectively communicate project development plans and study results to project teams and Senior level management.
• Team player who thrives in a high-speed environment where autonomy, accountability and innovation are critical for success.
• Excellent self-management and organizational skills, and ability to manage high volume workload.
• Clear and concise oral and written communication skills.
• Strong motivation, independence, and the ability to work in a multidisciplinary, matrix environment with minimal supervision.

Qualifications

• PhD in toxicology, pharmacology, or related scientific discipline
• 2+ years experience in small molecule and/or biopharmaceutical drug development desirable
• Or BS or MS, and extensive industry experience in nonclinical safety assessment; board certification or eligibility is desirable

Skills

• Good scientific expertise in subject area/discipline; familiar with other disciplines inside and/or outside of department (e.g., pathology, pharmacology, drug metabolism).
• Familiarity with ICH and GLP

Education

• PhD in toxicology, pharmacology, or related scientific discipline
• 2+ years experience in small molecule and/or biopharmaceutical drug development desirable
• Or BS or MS, and extensive industry experience in nonclinical safety assessment; board certification or eligibility is desirable