Clinical Research Nurse: Trial Coordination & Patient Care

Hannibal Regional Hospital; Hannibal (MO); On-site; USD 65,000 - 90,000; Full time

Job summary

Hannibal Regional Hospital is seeking a Clinical Research Nurse to lead clinical coordination and implement research studies. You will provide direct patient care in accordance with study protocols, GCP, and organizational policies, handling screening, consent, assessments, dosing, sample collection, and adverse event monitoring.

You will collaborate with the Clinical Research Coordinator, Principal Investigator, and the research team to ensure safe and compliant trials, while documenting

Qualifications

• Current licensure in Missouri as a Registered Nurse or ability to obtain
• Experience in Microsoft Word, Excel, and Outlook required
• Experience in phlebotomy required
• Experience placing IVs and giving infusions required
• Experience in clinical research preferred
• Highly effective verbal and written communication skills
• Ability to assess laboratory results and escalate clinically significant values
• Ability to follow detailed timelines for dosing, blood draws and assessments

Responsibilities

• Coordinate and implement clinical research studies within the organization
• Provide direct clinical care to research participants
• Screen and enroll participants and obtain informed consent
• Conduct clinical assessments and administer Investigational Product
• Collect specimens and monitor participant safety
• Document clinical research activities accurately
• Collaborate with the Clinical Research Coordinator and Principal Investigator
• Assist with study coordination and administrative tasks as needed

Skills

RN license

Phlebotomy

IV infusions

MS Word

MS Excel

Outlook

Clinical research experience

Verbal communication

Written communication

Tools

Microsoft Word

Microsoft Excel

Outlook

Job description

Hannibal Regional Hospital is seeking a Clinical Research Nurse to lead clinical coordination and implement research studies. You will provide direct patient care in accordance with study protocols, GCP, and organizational policies, handling screening, consent, assessments, dosing, sample collection, and adverse event monitoring.

You will collaborate with the Clinical Research Coordinator, Principal Investigator, and the research team to ensure safe and compliant trials, while documenting