Per Diem Clinical Research Nurse | Day Shift

IntelliResume; Hackensack (NJ); On-site; USD 55,000 - 96,000; Part time

Job summary

Hackensack Meridian Health is seeking a Clinical Research Nurse to coordinate and oversee clinical trial operations. The role requires a strong clinical nursing background and experience in research to support protocol development, regulatory submissions, and patient recruitment.

Responsibilities include working with principal investigators, IRB submissions, feasibility reviews, budget finalization, and patient assessment throughout trials.

Qualifications

• BSN required.
• Minimum of 3 years clinical nursing experience or 1 year of clinical nursing experience with an additional 2 years of clinical research experience.
• NJ State Professional Registered Nurse License
• AHA Basic Life Support (BLS) Certification within 60 days of starting
• National Certification in area of specialty preferred when eligible (e.g., CCRP/CCRP)
• CCRP/CCRA/CCRC certifications preferred

Responsibilities

• Assist the principal investigator in preparing proposed clinical trials.
• Ensure timely submission of protocol revisions and informed consents to the IRB.
• Act as liaison between principal investigators and sub-investigators on regulatory issues.
• Participate in feasibility review and evaluate potential competition.
• Finalize budget drafts with the budget coordinator.
• Recruit and evaluate potential study patients.
• Review medical records for potential study patients.
• Instruct patients and caregivers on aspects of care and trial procedures.
• Document study patients' medical history per protocol guidelines.
• Perform nursing assessments and monitor patients' progress during trials.

Skills

Clinical nursing

Regulatory coordination

IRB submissions

Study recruitment

Education

BSN

Job description

Hackensack Meridian Health is seeking a Clinical Research Nurse to coordinate and oversee clinical trial operations. The role requires a strong clinical nursing background and experience in research to support protocol development, regulatory submissions, and patient recruitment.

Responsibilities include working with principal investigators, IRB submissions, feasibility reviews, budget finalization, and patient assessment throughout trials.