Clinical Research Nurse: Trial Coordination & Protocols

Fairview Health Services; Saint Paul (MN); On-site; USD 82,000 - 115,000; Full time

Job summary

Fairview Health Services, based in Minnesota, seeks a Clinical Research Coordinator to support investigator-led studies. You will partner with the Recruitment team to screen participants, review protocols, and prepare regulatory materials and budgets.

The role requires an Associate's Degree in Nursing with 2 years clinical nursing and 2 years Clinical Research experience. You will ensure participant safety, obtain informed consent, and contribute to site initiation and ongoing study

Qualifications

• Requires Associate's Degree in Nursing.
• Minimum 2 years clinical nursing experience.
• Minimum 2 years Clinical Research experience.
• 1-5 years research experience.
• BLS certification.
• CCRCP and CCRP certifications desirable.

Responsibilities

• Partner with Recruitment to develop screening tools for participants.
• Analyze study protocol to support budget/contract negotiations.
• Prepare regulatory documents including IRB applications and informed consent.
• Educate internal and external parties on study protocols.
• Ensure participant safety and adherence to Good Clinical Practices (GCP).
• Assist with site initiation meetings and follow-up visits as per protocol.

Skills

Clinical nursing experience

Clinical research experience

Research coordination

Education

Associate's Degree in Nursing

BSN degree

Job description

Fairview Health Services, based in Minnesota, seeks a Clinical Research Coordinator to support investigator-led studies. You will partner with the Recruitment team to screen participants, review protocols, and prepare regulatory materials and budgets.

The role requires an Associate's Degree in Nursing with 2 years clinical nursing and 2 years Clinical Research experience. You will ensure participant safety, obtain informed consent, and contribute to site initiation and ongoing study