🛠 Tech Stack

💼 About This Role

You'll monitor clinical trials to ensure compliance with ICH/GCP guidelines and study protocols, acting as the key link between sponsors and site staff. Your core impact will be delivering high-quality trial execution across assigned studies, from site selection to close-out. This role offers the chance to join a rapidly growing company focused on early cancer detection.

🎯 What You'll Do

• Conduct site qualification, initiation, routine monitoring, and close-out visits.
• Provide ongoing guidance and performance oversight to investigative sites.
• Review, query, and reconcile clinical data; ensure timely resolution of issues.
• Ensure site documentation meets regulatory and audit readiness standards.

📋 Requirements

• 3+ years of clinical research experience including on-site and remote monitoring.
• Prior experience as a CRA within sponsor, biotech, or CRO environment.
• Bachelor's degree in life sciences, nursing, pharmacy, or related field.
• Strong knowledge of ICH-GCP and regulatory requirements.

✨ Nice to Have

• Experience in Oncology.
• Proficiency in CTMS, EDC, eTMF, and common clinical systems.

🎁 Benefits & Perks

• ✈️ 22 days PTO plus carryover option and birthday off.
• 🏥 Medical, dental, vision insurance plus life, STD, LTD, and 401(k).
• 🕒 Flexible work schedule.

🚩 Heads Up

• Requires 50-70% travel nationwide.
• Some responsibilities are duplicated in the listing.