💼 About This Role

You'll serve as a scientific and strategic leader, bridging discovery and clinical development for Tarsus Pharmaceuticals. Your core impact is driving pipeline programs from concept through IND-enabling and early clinical studies. This role offers the chance to build out toxicology and bio-analytics capacity in a hybrid/remote-friendly environment.

🎯 What You'll Do

• Serve as subject matter expert in toxicology across all programs.
• Oversee GLP and non-GLP toxicology studies at CROs.
• Author and review toxicology sections for regulatory submissions.
• Partner with internal teams and external partners for asset evaluation.

📋 Requirements

• PhD, MD/PhD, DVM, or related field in Toxicology or Pharmacology.
• 12+ years in pharma or biopharma toxicology/pathology.
• Strong GLP and ICH guidance knowledge.
• Experience with EMA/FDA CTA/IND submissions.

✨ Nice to Have

• DABT or ERT certification.
• Experience in ophthalmology.
• Experience managing outsourced studies.

🎁 Benefits & Perks

• 🏋️ Onsite gym
• 🏊 Pool
• 🍿 Snacks and drinks
• 🍽️ Occasional catered meals
• 📈 Bonus and stock equity

📨 Hiring Process

Estimated timeline: 2-4 weeks · AI estimate

1. 1Recruiter Call· 30 min
2. 2Technical Interview· 60 min
3. 3Final Interview· 60 min