🛠 Tech Stack

💼 About This Role

You'll serve as the primary coordinator for assigned clinical trials, managing study activities from start-up through closeout. You'll lead patient visits and maintain audit-ready documentation, directly impacting patient safety and data integrity. This role offers ownership of your studies and career growth.

🎯 What You'll Do

• Serve as primary coordinator for assigned clinical trials
• Manage study activities from start-up through closeout
• Lead interactions with study participants
• Maintain audit-ready documentation
• Work directly with investigators, sponsors, and CROs

📋 Requirements

• Clinical research coordination experience (2-3 years)
• Knowledge of ICH-GCP guidelines
• Experience with regulatory submissions and IRB processes
• Proficiency in electronic data capture systems

✨ Nice to Have

• Certification as a Clinical Research Coordinator (CCRC)
• Experience in oncology or internal medicine trials
• Familiarity with site management workflows

🎁 Benefits & Perks

• 🏖️ Paid Time Off
• 🏥 Health insurance
• 📚 Professional development opportunities
• 💰 Competitive compensation

📨 Hiring Process

Estimated timeline: 2-4 weeks · AI estimate

1. 1Recruiter phone screen· 30 min
2. 2Hiring manager interview· 45 min
3. 3On-site interview· 60 min