Inside Higher Ed
Study Coordinator
Location:
Chapel Hill, NC (UNC Medical Center, UNC Chapel Hill Campus, and satellite clinics)
Position type:
Permanent Staff (SHRA)
Salary range:
$63,875 - $75,100
Hours:
40 per week, Monday – Friday, 8:30 AM – 5:00 PM
Deadline:
January 22, 2026
Position Summary 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 (GCP), and institutional policies. The Coordinator independently manages multiple complex trials throughout their life cycle, including activation, implementation, and closure, under the direction of a Clinical Operations Manager.
Key Responsibilities
Recruit, consent, and enroll study participants.
Coordinate study visits across various clinic settings.
Document procedures and visits, facilitate sample collection, and perform data entry.
Collaborate with research teams to ensure regulatory compliance and patient safety.
Minimum Education and Experience Requirements Bachelor’s degree in a discipline related to clinical research and one year of related training or experience; or equivalent combination of training and experience. All degrees must be from accredited institutions.
Required Qualifications, Competencies and Experience
Knowledge of ICH GCP, Federal Regulations and Guidelines and ability to follow established 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.
Strong decision making and problem‑solving skills.
Customer‑oriented and ability to work in a team environment.
Effective verbal and written communication skills.
Study coordinator experience or experience in oncology clinical trials.
Availability to work on site at UNC Medical Center, UNC Chapel Hill Campus, and satellite clinics.
Availability for occasional evenings, weekends, and holidays.
Preferred Qualifications, Competencies and Experience
Experience with therapeutic clinical research involving drugs and/or devices.
Experience with direct patient contact in hospital/clinic setting.
SOCRA/ACRP certification.
Experience in Phase I, II, and III clinical research.
Familiarity with medical terminology, medical records, and data abstraction.
Prior experience with translational science research projects.
Demonstrated ability to operate independently.
Demonstrated ability to coordinate studies of high complexity.
Work Schedule and Requirements Clinic – UNCH or ACC, evening work occasionally; exposure to bloodborne pathogens, hazardous materials, laboratory work; overtime occasionally; patient care involved; weekend work occasionally.
About the University and Benefits University of North Carolina at Chapel Hill is a globally recognized higher education leader. Employees enjoy a comprehensive benefits package, paid leave, health, life and retirement plans, and a variety of programs supporting a healthy work/life balance. The campus offers professional training opportunities, exclusive perks, and a vibrant community culture.
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Chapel Hill, NC (UNC Medical Center, UNC Chapel Hill Campus, and satellite clinics)
Position type:
Permanent Staff (SHRA)
Salary range:
$63,875 - $75,100
Hours:
40 per week, Monday – Friday, 8:30 AM – 5:00 PM
Deadline:
January 22, 2026
Position Summary 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 (GCP), and institutional policies. The Coordinator independently manages multiple complex trials throughout their life cycle, including activation, implementation, and closure, under the direction of a Clinical Operations Manager.
Key Responsibilities
Recruit, consent, and enroll study participants.
Coordinate study visits across various clinic settings.
Document procedures and visits, facilitate sample collection, and perform data entry.
Collaborate with research teams to ensure regulatory compliance and patient safety.
Minimum Education and Experience Requirements Bachelor’s degree in a discipline related to clinical research and one year of related training or experience; or equivalent combination of training and experience. All degrees must be from accredited institutions.
Required Qualifications, Competencies and Experience
Knowledge of ICH GCP, Federal Regulations and Guidelines and ability to follow established 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.
Strong decision making and problem‑solving skills.
Customer‑oriented and ability to work in a team environment.
Effective verbal and written communication skills.
Study coordinator experience or experience in oncology clinical trials.
Availability to work on site at UNC Medical Center, UNC Chapel Hill Campus, and satellite clinics.
Availability for occasional evenings, weekends, and holidays.
Preferred Qualifications, Competencies and Experience
Experience with therapeutic clinical research involving drugs and/or devices.
Experience with direct patient contact in hospital/clinic setting.
SOCRA/ACRP certification.
Experience in Phase I, II, and III clinical research.
Familiarity with medical terminology, medical records, and data abstraction.
Prior experience with translational science research projects.
Demonstrated ability to operate independently.
Demonstrated ability to coordinate studies of high complexity.
Work Schedule and Requirements Clinic – UNCH or ACC, evening work occasionally; exposure to bloodborne pathogens, hazardous materials, laboratory work; overtime occasionally; patient care involved; weekend work occasionally.
About the University and Benefits University of North Carolina at Chapel Hill is a globally recognized higher education leader. Employees enjoy a comprehensive benefits package, paid leave, health, life and retirement plans, and a variety of programs supporting a healthy work/life balance. The campus offers professional training opportunities, exclusive perks, and a vibrant community culture.
#J-18808-Ljbffr