Social/Clinical Research Specialist

UNC-Chapel Hill • Chapel Hill, NC

14d

About The Position

This position serves as a Clinical Research Coordinator responsible for the operational management of multiple complex human subjects research studies within the UNC Department of Psychiatry’s Center for Women’s Mood Disorders. The Clinical Research Coordinator is responsible for the planning, organization, and conduct of multiple clinical research study protocols, including independently collecting and recording data, project administration, and communication with various stakeholders. The role supports both industry sponsored and non industry clinical trials involving psychiatric populations and requiring heightened regulatory oversight. The Coordinator manages studies across the full research lifecycle, including feasibility assessments, start up preparations, IRB and regulatory submissions, ongoing study conduct, monitoring readiness, and study closeout. The individual serves as a primary point of contact for operational activities, coordinating directly with sponsors, CROs, investigators, regulatory bodies, institutional partners, and research participants. The Coordinator will perform their duties using strong independent judgment, meticulous attention to regulatory and procedural detail, and the ability to anticipate and resolve operational challenges in a fast-paced research environment. Work Schedule Monday – Friday, 8am – 5pm, some evenings or weekends may be required.

Requirements

• Strong independent judgment
• Meticulous attention to regulatory and procedural detail
• Ability to anticipate and resolve operational challenges in a fast-paced research environment

Responsibilities

• Planning, organization, and conduct of multiple clinical research study protocols
• Independently collecting and recording data
• Project administration
• Communication with various stakeholders
• Managing studies across the full research lifecycle, including feasibility assessments, start up preparations, IRB and regulatory submissions, ongoing study conduct, monitoring readiness, and study closeout
• Coordinating directly with sponsors, CROs, investigators, regulatory bodies, institutional partners, and research participants

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Education Level: No Education Listed