Principal Investigator, MD

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