💼 About This Role

You'll support clinical trial operations at a community research site, partnering with physicians to offer patients access to new therapies. Your work ensures regulatory compliance and a smooth patient experience, directly improving lives through advanced treatment options. This role emphasizes compassion and excellence in a growing healthcare network.

🎯 What You'll Do

• Assist in coordinating clinical trial visits and procedures
• Maintain regulatory documents and study files
• Communicate with patients and study sponsors
• Ensure compliance with protocol and GCP guidelines

📋 Requirements

• Associate's degree in life sciences or related field
• 1-2 years of clinical research coordination experience
• Knowledge of ICH-GCP and FDA regulations
• Strong organizational and communication skills

✨ Nice to Have

• Bachelor's degree in a scientific discipline
• Certification (e.g., ACRP, SOCRA)
• Experience with electronic data capture systems

🎁 Benefits & Perks

• 🏖️ Paid time off and holidays
• 🏥 Medical, dental, and vision insurance
• 📈 401(k) with company match
• 📚 Professional development opportunities

📨 Hiring Process

Estimated timeline: 2-4 weeks · AI estimate

1. 1Recruiter phone screen· 30 min
2. 2Hiring manager interview· 45 min
3. 3Offer· 1 week