Physician - Clinical Trials - MD/DO

The role

The Principal Investigator or Sub-Investigator will lead and oversee clinical trials at a new research site. This role involves ensuring compliance with protocols, regulatory standards, and ethical guidelines while providing leadership to site staff.

What you will do

• Lead and oversee clinical trials conducted at Headlands Research sites
• Ensure compliance with protocol requirements, regulatory standards, and ethical guidelines
• Provide leadership and mentorship to site staff
• Participate in investigator meetings and educational initiatives
• Obtain IRB approval for study initiation and protocol modifications
• Oversee subject safety, trial conduct compliance, and the informed consent process
• Communicate effectively with sponsors, monitors, regulators, and research network leadership
• Provide ongoing training and support to research staff

Required qualifications

• Previous experience as a Principal Investigator or Sub-Investigator for clinical research trials
• Active and unencumbered license to practice as an MD or DO within the state of Tennessee
• Board-certified or board-eligible
• Excellent communication and leadership skills
• Familiarity with regulatory requirements, Good Clinical Practice (GCP) guidelines, and industry best practices in clinical research
• Strong organizational skills and attention to detail

Benefits

• Flexible Schedule

About the company

Headlands Research is a network of advanced clinical trial sites founded in 2018. The company operates 20+ sites across the US and Canada.