Clinical Research Coordinator I

Clinical Research Coordinator I assists investigators and study team in clinical research activities, adheres to research ethics and service values, and maintains regulatory documents. Prepares protocols, informed consents, and other necessary study documents for IRB and/or sponsor review. Maintains inventory of study supplies and equipment, prepares lab kits, and collects specimens from subjects.

Requirements

• Bachelor's degree required
• Good organizational skills
• Good verbal and written communications skills
• Some knowledge of FDA, HSR, and GCP Guidelines
• Proficient analytical skills

Benefits

• Medical, dental and vision insurance
• Employer paid group term life and disability
• Employer contribution toward Health Savings Account
• Flexible Spending Accounts
• Paid Time Off (PTO)
• Paid Holidays
• Paid Parental Leave
• 403(b) with a 5% employer match
• Tuition assistance
• Student loan servicing and support
• Adoption benefits
• Backup Childcare and Eldercare
• Employee Assistance Program
• Supplemental Life, AD&D and Disability
• Critical Illness, Accident and Hospital Indemnity coverage
• Discount on services at Lurie Children’s facilities
• Discount purchasing program