Clinical Research Nurse

Capitalmarketsp; Ohio; On-site; USD 65,000 - 70,000; Full time

Job summary

A prominent clinical research site in Columbus, OH is seeking a Clinical Research Nurse. This unique opportunity requires no prior research experience and offers a consistent schedule without nights or weekends. The role involves crucial patient support throughout clinical trials and a focus on the patient's well-being within a caring organizational culture.

Qualifications

• Must possess an RN degree.
• Willingness to learn and actively participate in clinical research.
• Ability to work on-site Monday to Friday.

Responsibilities

• Conduct vital signs, blood draws, EKGs, and infusions.
• Involved in patient recruitment, enrollment, and consent.
• Coordinate daily clinical trial activities and follow research protocols.

Skills

Patient Recruitment

Data Management

Communication

Education

RN degree

Job description

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• Unique opportunity to step into the clinical research industry -no prior research experience required!
• Consistent schedule, no overnights or weekends, flex holidays, and more!
• Work with a company that truly cares about their employees and patients
  
  

Highlights

• $65,000 - $70,000 salary + benefits!
• Unique opportunity to step into the clinical research industry -no prior research experience required!
• Consistent schedule, no overnights or weekends, flex holidays, and more!
• Work with a company that truly cares about their employees and patients
  
  

About Our Client

Our client is a long standing clinical research site in the Columbus, OH area that takes a truly unique patient-centric, service-oriented, approach to clinical research. Their reputation for excellence has been built across over 20 therapeutic areas, over 15 physicians, and over 550 completed trials. They are looking to expand their team with a skilled RN seeking to get into the clinical research industry!

Responsibilities

As a Clinical Research Nurse, you will be a specialized research professional under the direction of the clinical Principal Investigator and Site Manager. While the PI and Site Manager are responsible for the overall design, conduct, and management of the clinical trial, you support, facilitate, and coordinate the daily clinical trial activities and play a critical role in the conduct of the study including supporting patients throughout the clinical trial process!

• Conduct procedures such as vital signs, blood draws, EKGs, bladder scans, and infusions
• Patient recruitment, enrollment, and consent
• Lab procedures, processing, and shipments
• Maintain GCP and follow research protocols
• Data management in EDC systems
• Communication with sponsors and vendors on trial activities and patient care
• Overall coordination of the study
  
  

Qualifications:

• RN degree
• Willingness to work hands on and learn clinical research!
• Ability to work on site M-F on site (there is no remote or hybrid days)

Seniority level

• Seniority level

  Not Applicable

Employment type

• Employment type

  Full-time

Job function

• Job function

  Health Care Provider

• Industries

  Staffing and Recruiting

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