Hybrid Research Nurse Coordinator — Clinical Trials

Cleveland Clinic; Akron (OH); Hybrid; USD 63,000 - 96,000; Full time

Job summary

Cleveland Clinic Akron General Hospital is hiring a Research Nurse Coordinator to oversee the implementation and conduct of human subject research projects. You will apply nursing knowledge to develop care plans, perform evaluations, blood draws, EKGs, informed consent, and patient screening across disease areas.

The role includes regulatory activities, data entry using electronic data capture systems, and collaboration with investigators and central research administration to maintain protocol

Qualifications

• Graduate from an accredited school of professional nursing.
• Current state licensure as a Registered Nurse (RN).
• Basic Life Support (BLS) Certification through the AHA or ARC.
• Four years of clinical experience and two years of research experience.
• Basic computer proficiency.

Responsibilities

• Oversee implementation and conduct of human subject research projects in adherence to protocol requirements.
• Develop data, monitor plans, communicate regulatory documents, and report adverse events.
• Serve as liaison between investigators, study personnel and research administration.
• Assess subjects, perform nursing assessments, document findings and notify physicians of abnormal results.
• Coordinate ongoing care, discharge planning and patient safety within the research setting.
• Perform telephone triage and nursing procedures; manage informed consent and screening.
• Maintain standards of care per agency policies and assist with equipment as required.
• Assist with study design, protocol development and budget considerations.

Skills

Registered Nurse (RN)

BLS Certification

Clinical experience

Research experience

Education

RN licensure

BSN preferred

Job description

Cleveland Clinic Akron General Hospital is hiring a Research Nurse Coordinator to oversee the implementation and conduct of human subject research projects. You will apply nursing knowledge to develop care plans, perform evaluations, blood draws, EKGs, informed consent, and patient screening across disease areas.

The role includes regulatory activities, data entry using electronic data capture systems, and collaboration with investigators and central research administration to maintain protocol