Clinical Research Study Coordinator

Description

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Clinical Research Study Coordinator

The Urology Group is searching for a RN to work in the Clinical Research department to conduct pharmaceutical and device clinical trials in our office located in Norwood. The position is full time Monday through Friday, no nights, no weekends, no holidays.

Duties include:

• Recruit patients for participation in clinical trials
• Conduct patient visits, perform blood draws, check vital signs
• Perform Infusions and instillations of study medication
• Meet with sponsors during monitoring visits and attend internal and external meetings as needed

Benefits we offer:

• No nights, weekends or holidays
• 3 weeks PTO
• Medical/dental/vision insurance
• Company provided scrubs
• Short-term & long-term disability insurance
• Life and accident insurance
• 401k
• $2000 referral bonus potential

Requirements

 Requirements:

• Valid Ohio RN license
• Previous experience conducting clinical trials is preferred
• Certified Clinical Research Coordinator is ideal
• Must have excellent communication skills, be meticulous, able to work on their own and also cooperatively within a team environment.