Physician - Clinical Trials - MD/DO

The role

The Principal Investigator or Sub-Investigator will lead and oversee clinical trials at research sites. 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 New York
• 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.