Nurse Practitioner/PA/Sub-Investigator

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

We’re looking for a compassionate and experienced Nurse Practitioner to support our clinical research team in conducting Phase 2–4 trials, with a particular focus on metabolic conditions and GLP-1 therapies. If you thrive in a collaborative, patient-centered environment and are passionate about research-driven care, we’d love to meet you.

At Civia Health, you're not just taking a job: You're joining a mission to transform the way clinical research is done. Our purpose is bold: to bring clinical trials front and center in your community, make them accessible to everyday people, and empower underrepresented communities to participate.

We’re reinventing how clinical studies are run, delivering valid, scalable evidence with a consumer-first mindset. Too often, trials are expensive, fragmented, and overlook the experience of the participant. At Civia, we’re changing that. Our leadership team are experienced industry leading, visionary professionals who know what’s broken — and how to fix it.

We treat participants like valued partners, not research subjects. That means supporting their agency, putting their needs, comfort, and enjoyment first — and rewarding them generously for their time and effort.

What It Means to Work at Civia

Every team member plays a crucial role in reshaping clinical research. You’ll help make studies more human-centered, inclusive, and efficient. We're looking for people who are driven by purpose, inspired by innovation, and ready to roll up their sleeves to do meaningful work.

At Civia, your contributions aren’t just transactional, they’re transformational.

What You’ll Do

• 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, answering questions, 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.

What You Bring

• Active, unrestricted Nurse Practitioner license or Physician's Assistant license.
• 2+ years of clinical research experience (Phase 2–4 trials preferred).
• Experience with GLP-1 therapies or metabolic/endocrine research highly preferred.
• Strong knowledge of GCP/ICH guidelines; certification is a plus.
• Excellent clinical judgment, attention to detail, and communication skills.
• A collaborative spirit and commitment to doing what’s best for the patient and the team.

What We Offer

• Competitive compensation
• Medical, dental, and vision insurance
• Generous PTO and paid holidays
• Professional development and continuing education support
• A mission-driven team that values respect, inclusion, and innovation

Ready to Make an Impact?

• Mission with Meaning: Be part of a purpose-led team committed to health equity and real-world impact.
• Startup Energy, Proven Expertise: Work fast, adapt quickly, and help build something new; guided by seasoned visionary professionals who’ve seen what needs to change.
• People First Culture: We care deeply about our patients, participants, and each other. Collaboration, transparency, and bold, straight-talking are core to how we work.
• Invested in Your Growth: We don’t just hire for today; we’re building the leaders and changemakers of tomorrow.