Civia Health→
Principal Investigator, MD at Civia Health in Greenville, SC
Skills
Job Description
Reports to: Medical Director
Join Us at Civia Health
At Civia Health, we’re reimagining how clinical trials are delivered—by putting patients first and empowering providers to lead innovation. We’re seeking an experienced and compassionate Principal Investigator (PI) to oversee Phase 2–4 clinical trials in a collaborative, mission-driven environment. You’ll play a vital role in ensuring scientific integrity, patient safety, and regulatory compliance while contributing to groundbreaking research.
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
Serve as the physician of record and lead clinical oversight for assigned trials.
Review and approve study protocols, informed consent documents, and source documentation.
Conduct physical exams, medical reviews, and oversee safety assessments for participants.
Ensure compliance with all ICH-GCP, FDA, and IRB regulations.
Provide guidance and mentorship to the clinical research team.
Engage with sponsors, monitors, and regulatory bodies as needed.
Occasional travel may be required for audits, site visits, or team meetings.
What You Bring
Medical degree (MD or DO) with active and unrestricted license.
3+ years of experience as a Principal Investigator in clinical research (Phase 2–4 preferred).
Board certification in internal medicine, endocrinology, or related field preferred.
Strong working knowledge of GCP, FDA regulations, and clinical operations.
Excellent leadership, communication, and problem-solving skills.
Passion for innovation, ethics, and patient-centered care.
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?
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.
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 to the link above. We’re excited to learn more about you!