Study Coordinator

Job description

Position Type:

Permanent Staff (SHRA)

Is this an internal only recruitment?:


Position Title:

Soc/Clin Research Specialist - Journey

Working Title:

Study Coordinator

Position Number:

20003581, 20038284, 20001033, 20007336 and 20022480

Vacancy ID:


Budgeted Hiring Range:

$53,772 – $59,616

Pay Band Information:

To learn more about the pay band for this branch and role, please see the Career Banding rates spreadsheet.

Salary Grade Equivalent:


Full-time/Part-time Permanent/Time-Limited:

Full-Time Permanent

Hours per week:


Work Schedule:

Monday – Friday; 8:00 a.m. – 5:00 p.m.

Department Name and Number:

LCCC - Clinical Trials-426806

Date First Posted:


Closing Date:


Position Location:

Chapel Hill, NC

Position Posting Category:

Research Professionals

Department Description:

The UNC Lineberger Comprehensive Cancer Center (LCCC), founded in 1975, is a National Cancer Institute (NCI)-designated comprehensive cancer center. The Center’s mission is to reduce cancer occurrence and death in North Carolina and the nation through research, treatment, training and outreach.

UNC Lineberger’s Clinical Protocol Office is a centralized resource that supports the clinical research efforts of Lineberger investigators, primarily through the design and conduct of therapeutic clinical trials. The Protocol Office provides administrative, regulatory, data management, and study coordination services to investigators throughout the development, approval and implementation processes of protocols conducted at UNC and its affiliate institutions. The Protocol Office is responsible for protecting the safety of patients participating in research, ensuring the quality of the research, and safeguarding the interests of the University. It also furnishes protocol-related information to health professionals and to the community at large.

Equal Opportunity Employer:

The University of North Carolina at Chapel Hill is an equal opportunity and affirmative action employer. All qualified applicants will receive consideration for employment without regard to age, color, disability, gender, gender expression, gender identity, genetic information, race, national origin, religion, sex, sexual orientation, or status as a protected veteran.

Position Description:


Lineberger Comprehensive Cancer Center’s Clinical Protocol Office is recruiting for 5 Social/Clinical Research Specialist (Study Coordinator) positions (20001033, 20003581, 20007336, 20022480, and 20038284). By applying to this posting you will be considered for all 5 positions.

The purpose of this position is to facilitate the conduct of oncology clinical trials, including subject and data management, according to federal regulations, Good Clinical Practice, and local and institutional policies. These responsibilities relate to the mission of the UNC/LCCC Protocol Office by maintaining the quality of research and by addressing patient safety and regulatory compliance which impact research quality and safeguard institutional integrity.

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.

Essential Skills, Knowledge and Abilities:

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; ability to plan work and coordinate multiple projects; 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 evenings, weekends and/or holidays occasionally required.

Preferred Qualifications:

Previous experience with therapeutic clinical research involving drugs and/or devices. Experience in Phase I, II, and III clinical research. Experience navigating medical records and data extraction. SOCRA/ACRP Certification. One plus years of study coordinator experience or experience in oncology clinical trials and one plus year of oncology study coordinator experience.

Position/Schedule Requirements:

Exposure to Bloodborne Pathogens, Laboratory, Overtime occasionally, Patient care involved, Weekend work occasionally

Stimulus/ARRA Funded:





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Job No:
Posted: 6/8/2021
Application Due: 9/6/2021
Work Type: Full Time