Nurse Practitioner — Metabolic Clinical Research Specialist

Civia Health, LLC.; Independence (MO); On-site; USD 85,000 - 110,000; Full time

Benefits offered by this job

Health insurance

PTO and paid holidays

Professional development support

Mission-driven team

Job summary

Civia Health, LLC in Independence, Missouri is seeking a compassionate Nurse Practitioner to support our clinical research team in Phase 2–4 trials focusing on metabolic conditions and GLP-1 therapies.

You will conduct study visits, partner with investigators, educate participants, document adverse events, ensure regulatory compliance, and help optimize study workflows. Travel may be required occasionally.

Qualifications

• Active, unrestricted NP license or PA license.
• 2+ years of clinical research experience (Phase 2–4 trials preferred).
• Experience with GLP-1 therapies or metabolic research preferred.
• Strong knowledge of GCP/ICH guidelines; certification is a plus.
• Excellent clinical judgment, attention to detail, and communication skills.

Responsibilities

• Conduct study visits including medical assessments, physical exams, and protocol-specific procedures.
• Partner with principal investigators and research staff to ensure quality, safety, and regulatory compliance.
• Engage participants with empathy—providing clear education and ensuring comfort throughout the trial process.
• Identify, document, and report adverse events per protocol and regulatory standards.
• Maintain accurate, timely, and high-quality documentation in source records and EDC systems.
• Contribute to continuous improvement of workflows and study execution with a team-first mindset.
• Occasional travel may be required for audits, site visits, or team meetings.

Skills

Nurse Practitioner

Clinical research

Regulatory compliance

GLP-1 therapies

Education

NP/PA licensure

Tools

GCP/ICH guidelines

Job description

Civia Health, LLC in Independence, Missouri is seeking a compassionate Nurse Practitioner to support our clinical research team in Phase 2–4 trials focusing on metabolic conditions and GLP-1 therapies.

You will conduct study visits, partner with investigators, educate participants, document adverse events, ensure regulatory compliance, and help optimize study workflows. Travel may be required occasionally.