Provide global, end to end nonclinical safety leadership across multiple therapeutic areas and modalities, ensuring scientifically robust, fit for purpose, and regulatory compliant safety strategies
Job Summary
Provide global, end to end nonclinical safety leadership across multiple therapeutic areas and modalities, ensuring scientifically robust, fit for purpose, and regulatory compliant safety strategies.
Serve as the primary Preclinical Safety (PCS) authority on cross functional R&D teams and in interactions with global Health Authorities.
Compensation includes base salary, performance-based cash incentive, potential annual equity awards, and a comprehensive benefits package including health, life, disability, 401(k), and generous time off.
Matching Summary
Provide global, end to end nonclinical safety leadership across multiple therapeutic areas and modalities, ensuring scientifically robust, fit for purpose, and regulatory compliant safety strategies.
Salary
$185,500 - $344,500; Performance-based cash incentive and annual equity awards; Comprehensive benefits package including health, life, disability, 401(k), and generous time off
Skills & Requirements
Must-have
nonclinical safety leadership
global health authority interactions
drug development strategy
multiple therapeutic areas
multiple modalities
Nice-to-have
collaboration with BD&L
mentorship and coaching
advancing PCS objectives
Key Requirements
5+ years nonclinical safety Project Team experience
8+ years nonclinical drug development experience
Advanced scientific degree (PhD, MD, DVM, PharmD) or equivalent
Demonstrated expertise across multiple modalities
Proven track record of direct Health Authority interaction
Demonstrated leadership in matrix managed environments