💼 About This Role

You'll monitor and manage clinical studies at investigative sites, ensuring compliance with protocols and regulations for a smaller, specialized CRO. Your impact includes coordinating site activities and contributing to oncology trials that bring life-changing therapies to patients. This role offers reasonable travel and strong work-life balance.

🎯 What You'll Do

• Monitor progress of clinical studies at investigative sites
• Coordinate site setup activities like investigator identification and regulatory submissions
• Ensure studies are conducted per protocol, SOPs, ICH-GCP, and regulations
• Identify potential study risks and propose mitigation solutions

📋 Requirements

• Life science degree or equivalent experience
• 1 year or more as a CRA in CRO or pharma/biotech
• Oncology monitoring experience
• Availability for domestic travel up to 50-60%