💼 About This Role

You'll be the primary contracts professional for clinical site agreements and ancillary contracts across Nuvalent's global study portfolio. You'll work closely with Clinical Operations to manage the full lifecycle of CTAs, CDAs, and HCP consulting agreements. This role offers significant autonomy within a growing contracts department supporting four concurrent studies including a Phase 3 trial.

🎯 What You'll Do

• Draft, review, and negotiate Clinical Trial Agreements with global sites.
• Manage contract lifecycle from draft to execution and close-out.
• Coordinate Informed Consent Form review for site-level contracting.
• Negotiate Work Orders and Change Orders with CROs and vendors.

📋 Requirements

• 7+ years contracts experience in biopharma or clinical research.
• 4+ years focused on clinical site or vendor agreements.
• Experience negotiating CTAs, WOs, CDAs, and HCP agreements at volume.
• International clinical site contracting experience including GDPR knowledge.

✨ Nice to Have

• Agiloft contract management experience.
• Oncology therapeutic area experience.
• AI-assisted contract review tool familiarity.

🎁 Benefits & Perks

• 💰 Competitive Pay Transparency salary range $155K-$175K.
• 🏖️ Remote work with virtual environment support.
• 🏢 Growing contracts department with career advancement potential.
• 📈 Autonomy and collaboration with experienced teams.
• 🎓 On-the-job training on Agiloft and other tools.

📨 Hiring Process

Estimated timeline: 2-4 weeks · AI estimate

1. 1Recruiter screen· 30 min
2. 2Hiring manager interview· 45 min
3. 3Technical/contract negotiation assessment· 60 min