Study Coordinator

UNC-Chapel Hill • Chapel Hill, NC

5d • Onsite

About The Position

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.

Requirements

• Knowledge of ICH GCP , Federal Regulations and Guidelines and ability to follow established regulations, procedures, and protocols
• Strong computer skills
• Ability to gather data and document procedures
• High level of accuracy and attention to detail
• Ability to plan work and coordinate multiple projects
• Possess strong decision making and problem-solving skills
• Customer oriented and ability to work in a team environment
• Ability to communicate effectively and professionally verbally and in writing.
• Requires study coordinator experience or experience in oncology clinical trials
• 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.

Nice To Haves

• 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

Responsibilities

• 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

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Education Level: No Education Listed
• Number of Employees: 11-50 employees