🛠 Tech Stack

💼 About This Role

You'll oversee clinical trial monitoring at investigative sites, ensuring compliance and data integrity. You'll independently manage sites and collaborate with cross-functional teams to support enrollment and resolve operational challenges. This role offers the chance to work on complex clinical trials in a clinical-stage biotech with a life-saving mission.

🎯 What You'll Do

• Conduct site qualification, initiation, monitoring, and closeout visits
• Independently manage investigative sites and ensure protocol compliance
• Perform source data verification and review case report forms
• Train site staff on protocol procedures and GCP compliance

📋 Requirements

• Bachelor's degree in life sciences, nursing, or related field
• 4+ years clinical monitoring experience in pharma/biotech/CRO
• Experience managing academic medical center sites with limited IND experience
• Experience with eTMF, CTMS, and EDC systems

✨ Nice to Have

• Advanced degree preferred
• Experience with complex trials in critically ill or high-acuity populations (e.g., gene/cell therapy or transplant)

🎁 Benefits & Perks

• 🏖️ Flexible hybrid work
• 💰 Competitive base salary ($105,600-$158,400)
• 🏥 Comprehensive benefits package (likely standard for biotech)