Join Us at Civia Health
We’re looking for a compassionate and experienced Sub-Investigator 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.
Job Type: on-site
Reports to: Medical Director
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 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.
* 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
* Flexible scheduling options
* Professional development and continuing education support
* A mission‑driven team that values respect, inclusion, and innovation
Ready to make an impact? If you’re ready to be part of something meaningful—and work with people who care deeply about doing good work—apply today by submitting your resume and cover letter via the link above. We’re excited to learn more about you!
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