- Ph.D. in toxicology, pharmacology, physiology, biology, or related discipline.
- 6+ years of relevant nonclinical/toxicology experience in pharmaceutical or biotech drug development, with demonstrated experience representing toxicology on cross-functional project teams in a matrixed environment.
- DABT certification strongly preferred.
- Direct experience with small-molecule programs; working knowledge of the different evidence streams in nonclinical safety assessment.
- Strong understanding of the applicable safety evaluation framework (e.g., applicable ICH and OECD guidelines) and GLP.
- Track record designing and critically evaluating GLP toxicology, DART, and genotoxicity studies, and managing CRO relationships and deliverables.
- Strong written and oral communication skills; ability to translate complex toxicology data into clear risk-benefit guidance for non-toxicologist stakeholders.
- Ability to work collaboratively across cross-functional teams and under the guidance of the senior toxicology leadership.
- Highly organized and detailed oriented individual capable of managing multiple priorities.
- General scientific computer and software application proficiency.
Salary range: $150,000-$200,000, title and salary commensurate with experience.
Our Benefits: We are proud to offer health benefits, a discretionary bonus plan, stock option grants. a stock purchase plan, a 401(k) with match and paid time off to our team members as part of their compensation plan.
There is no deadline because the employer accepts applications on an ongoing basis.
Edgewise does not accept resumes from recruitment agencies for this position. Please do not send resumes to Edgewise employees or the company location. Edgewise is not responsible for any fees related to unsolicited resumes.