💼 About This Role

You'll lead nonclinical safety assessment for small molecule programs from discovery through IND stages. You'll work hands-on in the lab and oversee CRO studies to drive regulatory submissions. This role offers scientific independence in a fast-paced biotech environment.

🎯 What You'll Do

• Design and execute nonclinical safety studies with hands-on lab work
• Oversee GLP/non-GLP studies at external CROs
• Collaborate with cross-functional teams on project progression
• Analyze data and contribute to regulatory documentation

📋 Requirements

• PhD or MS in Toxicology or related discipline
• 5+ years industry experience in nonclinical safety assessment
• Experience from discovery through IND-enabling stages

✨ Nice to Have

• Experience with in vitro 3D models or safety screening platforms
• Familiarity with New Approach Methodologies (NAMs)
• CRO oversight experience

🎁 Benefits & Perks

• 💵 Competitive salary $160k-$220k
• 🏢 Downtown Boston office with hybrid flexibility
• 🔬 Hands-on lab work with cutting-edge technologies

📨 Hiring Process

Estimated timeline: 2-4 weeks · AI estimate

1. 1Recruiter Screen· 30 min
2. 2Hiring Manager Interview· 45 min
3. 3Technical Presentation· 60 min