CLINICAL RESEARCH COORDINATOR I

About this role

• * **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

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