🛠 Tech Stack

💼 About This Role

You'll support clinical operations for Kymera's TPD pipeline, coordinating logistics and maintaining eTMF in inspection-ready state. Your work ensures timely trial delivery and regulatory compliance. Collaborate across teams to drive innovative protein degrader therapies.

🎯 What You'll Do

• Maintain eTMF in inspection-ready state through ongoing QC and reconciliation.
• Review monitoring visit reports, study plans, and essential documents.
• Manage trial vendor oversight and vendor contracts.
• Lead eTMF archiving and coordinate file transfer at study closeout.

📋 Requirements

• BS/BA degree; scientific or health-related field preferred.
• 3+ years clinical trial experience with at least one year on sponsor side.
• Knowledge of ICH and GCP guidelines.
• Experience building and managing external contract research relationships.

🎁 Benefits & Perks

• 💰 Annual bonus eligibility.
• 📈 Equity participation.
• 🏥 Comprehensive benefits package.

📨 Hiring Process

Estimated timeline: 2-4 weeks · AI estimate

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