Study Coordinator

This position plays a pivotal role in advancing cancer research and improving patient outcomes by facilitating the conduct of oncology clinical trials in compliance with federal regulations, Good Clinical Practice, and institutional policies. This position independently manages multiple complex trials throughout their life cycle, including activation, implementation, and closure, under the direction of a Clinical Operations Manager.

Key responsibilities include :

• Recruitment, consent, and enrollment of study participants
• Coordination of study visits across various clinic settings
• Documentation of procedures and visits, facilitation of sample collection, and data entry
• Collaboration with research teams to ensure regulatory compliance and patient safety

This position is integral to the mission of the UNC / LCCC Clinical Trials Office, maintaining research quality and safeguarding institutional integrity, and driving discoveries that shape the future of cancer care. Minimum Education and Experience Requirements Bachelor’s degree in a discipline related to the field assigned and one year of related training or experience; or equivalent combination of training and experience. All degrees must be received from appropriately accredited institutions. Management Preferences This posting was approved prior to the state mandated discontinued use of “Required Qualifications, Competencies, and Experience”. Postings initially approved prior to 1 / / 6 will fall under previous review and selection policies.

Required Qualifications, Competencies, and Experience

High level of accuracy and attention to detail,

Ability to work on site at UNC Medical Center, UNC Chapel Hill Campus, and any satellite clinic site where trials are conducted.

Ability to work on evenings, weekends and / or holidays occasionally required.

Preferred Qualifications, Competencies, and Experience

Previous experience with therapeutic clinical research involving drugs and / or devices

Experience with direct patient contact in the hospital / clinic setting

SOCRA / ACRP Certification

Experience in Phase I, II, and III clinical research.

Experience or familiarity with medical terminology, navigation of medical records and data abstraction

Prior experience with translational science research projects

Demonstrated ability to operate at a high degree of independence

Demonstrated ability to coordinate studies of high complexity Required Licenses / Certifications Special Physical / Mental Requirements Campus Security Authority Responsibilities