Nurse Practitioner/Sub-Investigator

Civia Health•Independence, MO

2d•Onsite

About The Position

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. 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.

Requirements

Active, unrestricted Nurse Practitioner license in Missouri.
2+ years of clinical research experience (Phase 2–4 trials 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.

Nice To Haves

Experience with GLP-1 therapies or metabolic/endocrine research highly preferred.

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, 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.