Employment Type : Full-Time
Position Type Permanent Staff (SHRA)
Is this an internal only recruitment? No
Position Title Soc/Clin Research Assistant - Journey
Working Title Data Coordinator
Position Number 20014663 and 20028515
Vacancy ID P012833
Budgeted Hiring Range $40,945 - $47,000
Pay Band InformationTo learn more about the pay band for this branch and role, please see the Career Banding rates spreadsheet.
Salary Grade Equivalent GN08
Full-time/Part-time Permanent/Time-Limited Full-Time Permanent
If time-limited, estimated duration of appointment
Hours per week 40
Work ScheduleMonday-Friday; 8:30 a.m. to 5:00 p.m.
Department Name and Number LCCC - Clinical Trials-426806
Date First Posted 05/27/2021
Closing Date 08/18/2021
Position Location Chapel Hill, NC
Position Posting Category Research Professionals
Department DescriptionThe UNC Lineberger Comprehensive Cancer Center, 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 EmployerThe 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 DescriptionTHIS IS A REPOST. PREVIOUS APPLICANTS ARE STILL BEING CONSIDERED AND NEED NOT REAPPLY.
Lineberger Comprehensive Cancer Center’s Clinical Protocol Office is recruiting for two (2) Social/Clinical Research Assistant (Data Coordinator) positions (20014663 and 20028515). By applying to this posting you will be considered for both positions.
This position will independently coordinate complex clinical research studies and perform site initiation activities, help create data collection forms, and coordinate the comprehensive protocol patient record charts by supervising collection of all inter-departmental data records for assigned studies. Additionally, the position will independently assess patients for eligibility for inclusion in studies. The position will oversee the registration and randomizing of patients into studies and assure accurate data is documented in accordance with clinical research protocols and federal regulations. The position will oversee and/or perform the proper processing and shipping of patient laboratory samples for assigned protocols correctly according to procedures outlined in the protocol/laboratory manual in a timely fashion.
Minimum Education and Experience RequirementsBachelor’s degree; or equivalent combination of training and experience. All degrees must be received from appropriately accredited institutions.
Essential Skills, Knowledge and AbilitiesWorking knowledge of and facility with information technology; ability to organize and analyze information; ability to document procedures and to lead exchange of information through dialogue, instruction, and demonstration; ability to develop working knowledge of proprietary databases sufficient to ensure quality control and quality assurance tasks; ability to manage multiple tasks and projects; ability to develop working knowledge of compliance and procedures relating to oncology clinical research; and ability to communicate professionally both verbally and in writing.
Preferred QualificationsKnowledge and experience with data management and clinical research methods.
Required Licenses/Certifications
Special Physical and Mental Requirements
Position/Schedule Requirements Evening work occasionally, Exposure to Bloodborne Pathogens, Exposure to Hazardous Materials, Overtime occasionally
Position Attributes
Stimulus/ARRA Funded No
Quick Link https://unc.peopleadmin.com/postings/193360
Office of Human Resources