Physician Investigator Clinical Trials

About the Company

Triad Clinical Trials is an independent medical research clinic located in Greensboro, NC, near the campus of historic Guilford College. For over 15 years, our team has conducted high-quality clinical research and enrolled more than 5,000 Triad-area residents in a broad range of studies. As demand for clinical research continues to grow, we are seeking an experienced, licensed physician (MD or DO) to join our team as a Clinical Research Investigator.

About the Role

This is a permanent, part-time position requiring approximately 6–8 clinical hours per week (flexible; one weekday morning and one weekday afternoon). The Investigator will provide medical oversight and leadership for ongoing and upcoming clinical trials in Phases II–IV. The role involves evaluating participant safety, conducting study-related exams and assessments, and collaborating closely with our research staff and sponsor partners to ensure the highest standards of clinical and regulatory compliance.

Responsibilities

• Serve as Principal Investigator (PI) or Sub-Investigator for assigned clinical trials.
• Provide medical and scientific oversight throughout all stages of the study.
• Evaluate and determine study participant eligibility per protocol criteria.
• Conduct physical examinations and clinical assessments as required.
• Review diagnostic results and provide clinical interpretation and direction to the study team.
• Ensure protocol adherence and regulatory compliance with FDA, ICH, and GCP standards.
• Collaborate with internal teams in Clinical Operations, Regulatory Affairs, and Patient Engagement.
• Communicate study-related information clearly to participants and clinical staff.
• Complete all required sponsor and industry training in a timely manner.

Qualifications

• MD or DO, currently licensed to practice medicine in the State of North Carolina with no history of license suspension or debarment.
• 2+ years of experience as a clinical investigator on pharma-sponsored clinical trials (highly preferred).
• Board certification preferred.
• Excellent interpersonal and communication skills; ability to build rapport with study participants, sponsors, and team members.
• Strong attention to detail, organizational ability, and commitment to quality and compliance.

Why Join Us

• Flexible schedule (one weekday morning and one weekday afternoon, 6–8 hours/week).
• Opportunity to contribute to innovative research improving patient outcomes.
• Supportive, experienced clinical research team.
• Collaborative, community-focused environment with a strong reputation for excellence.

Equal Opportunity Statement

We are committed to diversity and inclusivity in our hiring practices and encourage applications from all qualified individuals.