Research Professor

UNC-Chapel Hill • Chapel Hill, NC

1d

About The Position

The Division of Endocrinology and Metabolism in the Department of Medicine at the University of North Carolina School of Medicine seeks a part-time, temporary research faculty member. The successful candidate will serve as a principal investigator (PI) for clinical research studies within the Endocrine Clinical Research Unit, with overall responsibility for ensuring studies are conducted in accordance with approved protocols, Good Clinical Practice, UNC institutional policies, and all applicable regulatory and IRB requirements. The PI will oversee participant safety, informed consent, adverse event reporting, and data integrity; supervise and appropriately delegate responsibilities to research staff; and serve as the primary point of contact with study sponsors and institutional stakeholders. Clinical responsibilities may include evaluating and managing research participants and covering shifts in the trials unit as needed.

Requirements

• Serve as a principal investigator (PI) for clinical research studies within the Endocrine Clinical Research Unit.
• Ensure studies are conducted in accordance with approved protocols, Good Clinical Practice, UNC institutional policies, and all applicable regulatory and IRB requirements.
• Oversee participant safety, informed consent, adverse event reporting, and data integrity.
• Supervise and appropriately delegate responsibilities to research staff.
• Serve as the primary point of contact with study sponsors and institutional stakeholders.
• Evaluate and manage research participants.
• Cover shifts in the trials unit as needed.

Nice To Haves

• Experience as the PI for industry-sponsored clinical trials

Responsibilities

• Serve as a principal investigator (PI) for clinical research studies within the Endocrine Clinical Research Unit.
• Ensure studies are conducted in accordance with approved protocols, Good Clinical Practice, UNC institutional policies, and all applicable regulatory and IRB requirements.
• Oversee participant safety, informed consent, adverse event reporting, and data integrity.
• Supervise and appropriately delegate responsibilities to research staff.
• Serve as the primary point of contact with study sponsors and institutional stakeholders.
• Evaluate and manage research participants.
• Cover shifts in the trials unit as needed.

What This Job Offers

• Job Type: Part-time
• Career Level: Principal
• Education Level: No Education Listed