💼 About This Role

You'll support clinical trial operations in internal medicine, coordinating with community physicians to provide patients access to advanced therapies. Your work ensures regulatory compliance and smooth study execution, directly improving patient care experiences.

🎯 What You'll Do

• Assist in coordinating clinical trial activities and patient visits
• Maintain regulatory documents and ensure compliance
• Collect and record study data accurately
• Communicate with patients and study team

📋 Requirements

• Bachelor's degree in a health-related field
• 1-2 years of clinical research coordination experience
• Knowledge of GCP and FDA regulations
• Certified Clinical Research Coordinator (CCRC) preferred

✨ Nice to Have

• Experience with electronic data capture systems
• Familiarity with IRB submissions
• Bilingual in Spanish

🎁 Benefits & Perks

• 🏖️ Competitive PTO
• 🏥 Health insurance
• 📚 Professional development opportunities

📨 Hiring Process

Estimated timeline: 2-4 weeks · AI estimate

1. 1Phone Screen· 30 min
2. 2In-Person Interview· 1 hour
3. 3Offer· N/A