Soc/Clin Research Specialist

Job description

Position Type:

Permanent Staff (SHRA)

Is this an internal only recruitment?:

No

Position Title:

Soc/Clin Research Specialist - Contributing

Working Title:

Soc/Clin Research Specialist

Position Number:

20037526

Vacancy ID:

P012204

Budgeted Hiring Range:

$46,000 - $51,000

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:

GN09

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

Full-Time Time-Limited

If time-limited, estimated duration of appointment:

2 years

Hours per week:

40

Work Schedule:

M-F, 8am-5pm.

Department Name and Number:

Biostatistics - CSCC-462002

Date First Posted:

12/10/2020

Closing Date:

03/12/2021

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 School of 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 (HCHS); and Preconceptional Health of Latinas and its Association with Child Adiposity (HCHS-FLOR). Information on these and other studies can be found at http://www.cscc.unc.edu/cscc/index.php

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 acts as 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 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 Contributing-level applied competencies of Technical Knowledge (clinical research principles and regulatory documentation and monitoring), Communication (preparation of data queries, reports and presentations of compiled results), Data/ Information Collection (organizing and collecting records, data entry, and archival) and Information and Records Administration (compilation, summary and report generation). The work requires use of sound evidence based judgement and research skills.

The position requires knowledge of applied aspects of observational study and/or clinical trial design, data analysis, research data management and reporting through education or work experience.

Candidates must have the ability to work independently with minimal supervision; strong attention to detail; and an ability to handle deadlines, flexibility with priorities, and ability to handle confidential information.

Proficiency with MS Word, PowerPoint, Excel, and other MS Office and electronic mail software, and experience with electronic informational resources (including the internet and informational databases) is required.

Preferred Qualifications:

The candidate will have experience in a research setting. Clinical and/or public health research study experience is preferred, particularly with data management development and implementation, enrollment tracking, and site monitoring tasks. Regulatory development and oversight experience is desirable.

Attention to detail and strong organizational skills are essential. Good written and oral communication skills, and the ability to work within a team are essential.

A Bachelor’s degree with two years of relevant research experience or a Master’ degree with at least one year of relevant research experience is preferred.

Proficiency in verbal and written Spanish.

Stimulus/ARRA Funded:

No

 

 

 

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Job No:
Posted: 2/17/2021
Application Due: 5/18/2021
Work Type: Full Time
Salary: