Soc/Clin Research Specialist

University of North Carolina- Chapel Hill

United States

September 17, 2021


Posting Information Position Type Permanent Staff (SHRA)

Is this an internal only recruitment? No Position Title Soc/Clin Research Specialist - Journey Working Title Soc/Clin Research Specialist Position Number 20020215 & 00013090 & 20020219 Vacancy ID P013374 Budgeted Hiring Range $50,146 - $72,826 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 GN11 Full-time/Part-time Permanent/Time-Limited Full-Time Permanent If time-limited, estimated duration of appointment Hours per week 40 Work Schedule

M-F, 8-5

Department Name and Number Biostatistics - CSCC-462002 Date First Posted 08/25/2021 Closing Date 09/17/2021 Position Location Chapel Hill, NC Position Posting Category Research Professionals

Department Description

The Collaborative Studies Coordinating Center (CSCC) is a division within the Department of Biostatistics of the Gillings School of Global Public Health at the University of North Carolina at Chapel Hill, NC (UNC). As the coordinating center for a number of multi-center clinical trials and epidemiology studies, the CSCC provides study design, data management, statistical analysis, quality assurance, and study management services to a broad array of projects funded primarily by the National Institutes of Health (NIH). The organization includes faculty from the departments of Biostatistics, Epidemiology, and Medicine and research staff with training and experience in biostatistics, epidemiology, computer science/data management, and project management. Total employees currently number between 100 and 105. The CSCC was established in 1971 as the Lipid Research Clinics (LRC) Coordinating Center and has operated continually since that time. To reflect the addition of new studies and expansion into new research areas, the LRC Coordinating Center changed its name to the Collaborative Studies Coordinating Center (CSCC) in 1984. Major research programs for which the CSCC currently serves as coordinating center include the Atherosclerosis Risk in Communities Study (ARIC); Adolescent Medicine Trials Network for HIV/AIDS Interventions (ATN); Back Pain Consortium (BACPAC) as part of the Helping to End Addiction Long-term Initiative (HEAL); Subpopulations and Intermediate Outcome Measures in COPD Study (SPIROMICS); Biological Underpinning of COPD Heterogeneity and Progression (SPIROMICS II); Precision Interventions for Severe and/or Exacerbation Prone Asthma Network (PrecISE); Hispanic Community Health Study/ Study of Latinos (HCHS/SOL); and Preconceptional Health of Latinas and its Association with Child Adiposity (HCHS-FLOR).

Information on these and other studies can be found at https:// www.

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.

Inclusive Excellence is a core value at the Gillings School of Global Public Health. We expect our faculty and staff to actively contribute to fostering an academic workplace climate that is welcoming and supportive for all.

Position Description

This Social/Clinical Research Specialist (SCRS) is a member of one or more research study teams managed by a Project Director and Principal Investigator (faculty). The position plays an important role in the operational support of research studies, where the CSCC is the primary Operations, Data Management, and Statistical Coordinating Center, and is responsible for supporting multiple activities within a project lifecycle such as: development, planning, coordination, and monitoring of clinical study conduct and data quality control.

The SCRS supports a variety of clinical and behavioral research activities, including but not limited to the conduct, facilitation and coordination of observational studies and clinical trials according to investigator or sponsor initiated protocols. The SCRS also helps in preparation/ submission of regulatory documents, clinical monitoring and study management processes in accordance with ICH Good Clinical Practices (GCP), FDA guidelines, and other regulations.

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

This position requires Journey-level applied competencies of Professional Knowledge (clinical research principles, methods and processes; methods of data collection and analysis; interpreting and reporting results; regulatory submissions, documentation and monitoring), Project Design (plan, organize, conduct, and/or evaluate social/clinical research), Project/Program Administration (manage and administer multiple projects, tasks, protocols, and timelines within a study or multiple studies), Communication (clear, concise and effective written and oral communication with all field staff and in-house staff and investigators), Data/Information Collection (coordinate data collection, monitoring and data management, prepare reports and presentations), and Instruction (develop and conduct training to field center staff and new in house staff). The work requires use of sound evidence based judgement and research skills.

This position requires a basic understanding of scientific principles, methods, results presentation and reporting. Knowledge of applied research in observational and/or clinical trial design, data analysis, research data management and reporting through education or work experience is required.

Candidates must have the ability to work independently with minimal supervision and work within a team; possess strong attention to detail and organizational skillls; the ability to prioritize deadlines, demonstrate flexibility with priorities, and handle confidential information.

Preferred Qualifications

Master's degree and at least two years of experience in research is preferred.

Required Licenses/Certifications Special Physical and Mental Requirements Position/Schedule Requirements Position Attributes Stimulus/ARRA Funded No Quick Link https: //

Office of Human Resources Contact Information

If you experience any problems accessing the system or have questions about the application process, please contact the Office of Human Resources at (919) 843-2300 or send an email to

Please note: The Office of Human Resources will not be able to provide specific updates regarding position or application status.

Applicant Documents

Required Documents

  • Curriculum Vitae / Resume
  • Cover Letter
  • List of References
  • Optional Documents

    Posting Supplemental Questions

    Required fields are indicated with an asterisk ().

  • Please select the response below that best describes your experience/education for the Social/Clinical Research Specialist position.
  • Bachelor's in a discipline related to the field assigned and at least 1 year of related training or experience.
  • Associate's, Bachelor's, Master's, Doctorate in an unrelated field and at least 5 years of related training and/or experience.
  • Master's and/or Doctorate in a discipline related to the field assigned.
  • Associate's in a discipline related to the field assigned and at least 3 years of related training or experience.
  • Combination of post-high school education and experience to equal at least 5 years of experience related to the field assigned (ex: 1 year towards a degree and 4 years experience).
  • Did not complete high school but have a combination of high school education and related experience to equal at least 9 years (ex. 3 years of high school and 6 years of experience).
  • None of the above
  • Do you have prior experience working for a coordinating center? If so, please describe your prior experience.
  • (Open Ended Question)

  • Do you have any previous clinical research experience? If yes, please describe briefly.
  • (Open Ended Question)

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