Patient-Centered PI (MD): Lead Clinical Trials

Civia Health, LLC.; Independence (MO); Hybrid; USD 180,000 - 240,000; Full time

Benefits offered by this job

Medical Insurance

Dental Insurance

Vision Insurance

PTO (Generous)

Professional development

Job summary

Civia Health, LLC. is seeking an experienced Principal Investigator to oversee Phase 2–4 clinical trials. You will ensure scientific integrity, patient safety, and regulatory compliance while guiding a collaborative research team in a mission-driven environment.

The successful candidate will hold an MD or DO, possess an active license, and have 3+ years as a PI in clinical research with strong knowledge of GCP and FDA regulations. Some travel may be required.

Qualifications

• MD or DO with active license
• 3+ years of PI experience in clinical research (Phase 2–4)
• Board certification in internal medicine, endocrinology, or related field preferred
• Strong knowledge of GCP, FDA regulations, and clinical operations
• Excellent leadership, communication, and problem-solving skills

Responsibilities

• 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

Education

MD/DO degree

Board certification in internal medicine or endocrinology

Job description

Civia Health, LLC. is seeking an experienced Principal Investigator to oversee Phase 2–4 clinical trials. You will ensure scientific integrity, patient safety, and regulatory compliance while guiding a collaborative research team in a mission-driven environment.

The successful candidate will hold an MD or DO, possess an active license, and have 3+ years as a PI in clinical research with strong knowledge of GCP and FDA regulations. Some travel may be required.