Clinical Research Coordinator II (Regulatory/Remote) - Medical Oncology

The Clinical Research Coordinator II assists investigators in developing plans for research projects, coordinates the development of forms, questionnaires, and research techniques, and ensures compliance with regulatory agencies. The position is responsible for managing all phases of study/protocol, including record-keeping, data analysis, and reporting of adverse events. The coordinator will also serve as a liaison with funding or sponsoring agencies, evaluate and interpret collected clinical data, and prepare presentations or reports setting forth progress trends and providing recommendations.

Requirements

• Bachelor’s degree or combination of education and/or experience
• Basic Life Support certification
• 2 years of clinical research experience
• Skills in clinical research, clinical study protocols, database management, research projects, spreadsheet analysis, and statistical analysis software (SAS)

Benefits

• Up to 22 days of vacation
• 10 recognized holidays
• Sick time
• Competitive health insurance packages
• Defined contribution (403(b)) Retirement Savings Plan
• Wellness challenges
• Annual health screenings
• Mental health resources
• Mindfulness programs and courses
• Employee assistance program (EAP)
• Financial resources
• Access to dietitians
• 4 weeks of caregiver leave
• Family care resources
• Tuition coverage for eligible employees and their families