Overview
We are partnered with an established clinical research site network seeking a Principal Investigator to support clinical trial activities in Nashville, Tennessee. The site partners with leading pharmaceutical sponsors and CROs to conduct Phase II–IV industry-sponsored studies and is looking to expand investigator coverage in their Nashville site.
Responsibilities
• Serve as Principal Investigator for assigned clinical trials
• Provide medical oversight to ensure subject safety and protocol compliance
• Review and approve study-related documentation
• Conduct protocol-required visits and assessments
• Supervise research staff and delegated duties
• Ensure adherence to GCP, FDA regulations, and site SOPs
• Participate in sponsor meetings, SIVs, and monitoring visits
• Support recruitment and retention strategies
• Maintain accurate and timely documentation
Qualifications
• MD or DO required
• Active and unrestricted Tennessee medical license (or willingness to obtain)
• Board certification or board eligible preferred
• Prior clinical research experience as a PI or Sub-I preferred
• Open to physicians across any therapeutic area
• Strong interest in clinical research
Preferred Experience
• Industry-sponsored clinical trials
• Dedicated research site experience
• GCP training
• Ability to commit consistent time to research
What’s Offered
• Flexible scheduling options
• Strong operational and regulatory support
• Access to sponsor relationships through a larger network
• Competitive compensation structure
• Long-term collaboration opportunities
