The Clinical Research Coordinator works collaboratively with multidisciplinary teams, research, and hospital staff to recruit, screen, educate, and assist in the overall clinical study coordination of clinical research.
Requirements
- Recruit and educate potential patients for and evaluate potential patient eligibility for clinical trials
- Maintain source documents and submit case report forms (CRFs) as required for clinical trials
- Recognize and report adverse events/serious adverse events to the Principal Investigator, FDA, and sponsors
Benefits
- Coverage begins on day one for health, dental, and vision insurance
- Employer-paid life insurance, long-term disability insurance, and various additional voluntary insurance plans
- Paid time off, including vacation and sick, begins accruing upon hire
- Ten paid holidays
- One paid discretionary day after six months of employment
- Paid time off for bereavement, jury duty, military service, and parental leave after 12 months of employment
- A retirement program with a generous employer contribution and additional voluntary retirement programs (457 or 403b)