What are the responsibilities and job description for the CLINICAL RESEARCH COORDINATOR I position at St. Bernards Healthcare?
- JOB REQUIREMENTS
- Education Required
- Associates Degree preferred
- Experience
- Experience in clinical setting required. 1 year of clinical research experience preferred.
- Physical
- This is a safety sensitive position. Please see the St. Bernards Substance Abuse Policy for further information.
- Requires – mobility, sight, hearing, verbal communication, changes in temperature, exposure to disagreeable elements (dusts, fumes, odors, water, etc.), exposure to biological, mechanical, electrical, and chemical hazards. Frequent standing, walking, bending, and stooping. Lifting up to 40 lbs. Carrying up to 40 lbs. Pushing/pulling up to 40 lbs. Close eye work. Hearing of normal and soft tones.
- JOB SUMMARY
- The Clinical Research Coordinator performs job duties as delegated by, and under the oversite of, the Principal Investigator. The CRC I coordinates studies of basic to moderate complexity and will serve as the primary point of contact for patients enrolled to studies under their management.
Location: St. Bernards Healthcare · CLINICAL TRIAL RESEARCH
Schedule: Full Time, Day Shift, M-F 8am-4:30pm
Benefits:
Health Insurance, Vacation & Paid Time Off, Maternity & Paternity LeaveSalary : $42,973 - $61,390