Clinical Research Coordinator

Job Summary

We are seeking an experienced Clinical Research Coordinator to support Phase I Oncology clinical trials. The ideal candidate will independently coordinate study activities, ensure regulatory compliance, and work closely with investigators, sponsors, and clinical teams.

Responsibilities

• Care for Phase I oncology clinical research studies
• Recruit, enroll, and retain study participants
• Manage study documentation, data collection, and regulatory submissions
• Ensure compliance with IRB, FDA, HIPAA, guidelines
• Collaborate with investigators, sponsors, and study monitors
• Report adverse events and maintain accurate study records

Required Qualifications

• Bachelor's degree in a related field or equivalent experience
• 2+ years of Clinical Research Coordinator experience
• Hands-on experience with Phase I Oncology treatment trials
• Experience working in a hospital or academic medical center
• Proficiency with EPIC EMR
• Strong knowledge of IRB, FDA regulations, HIPAA, and medical terminology
• Excellent communication and organizational skills

Benefits

• Medical insurance
• Dental insurance
• Vision insurance
• 401(k) retirement plan
• Life insurance
• Long-term disability insurance
• Short-term disability insurance
• Paid parking/public transportation
• (Paid time off, paid sick and safe time, hours of paid vacation time, weeks of paid parental leave, paid holidays annually - AS Applicable)