Clinical Research Nurse: Lead Trials & Patient Care

Mercy Co; Overland (MO); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Medical coverage

Dental coverage

Vision coverage

Paid time off

Tuition assistance

Retirement matching

Job summary

Mercy is seeking a Clinical Research Nurse to coordinate and manage clinical trials, ensuring patient safety and regulatory compliance throughout the study lifecycle. The CRN will recruit participants, monitor visits, collect data, and oversee investigational product handling in coordination with Mercy Research partners.

The role emphasizes training, collaboration with physicians and CROs, and adherence to Mercy's standards while supporting ongoing growth of the research program.

Qualifications

• Nursing education: Diploma, ADN, or BSN.
• Current RN license in the applicable state.
• Experience: BSN 2+ years; ADN or Diploma 3+ years; relevant experience may vary.
• Ability to perform patient assessments and clinical procedures (vital signs, ECGs, spirometry, phlebotomy) or willingness to learn.
• Strong communication and organizational skills; proficient in MS Office and electronic systems.
• Preferred: 2+ years clinical research experience; phlebotomy experience.

Responsibilities

• Coordinate and manage assigned clinical trials from start-up through completion.
• Conduct feasibility assessments and support initiation activities.
• Maintain knowledge of study protocols and ensure compliance with research requirements.
• Administer or oversee investigational medications and procedures per protocol.
• Partner with physicians, nurses, sponsors, and CROs to ensure study execution.

Skills

Patient assessment

Clinical procedures

Communication skills

Multitasking

Education

Nursing Diploma

ADN

BSN

Tools

Microsoft Office

Electronic systems

Job description

Mercy is seeking a Clinical Research Nurse to coordinate and manage clinical trials, ensuring patient safety and regulatory compliance throughout the study lifecycle. The CRN will recruit participants, monitor visits, collect data, and oversee investigational product handling in coordination with Mercy Research partners.

The role emphasizes training, collaboration with physicians and CROs, and adherence to Mercy's standards while supporting ongoing growth of the research program.