Data Coordinator

UNC-Chapel Hill

Chapel Hill (NC)

In loco

USD 45.000 - 60.000

Tempo pieno

2 giorni fa
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Descrizione del lavoro

University of North Carolina in Chapel Hill seeks a Clinical Research Assistant to independently coordinate data entry for oncology treatment trials and manage patient records in alignment with GCP and UNC policies.

The role requires a Bachelor’s degree with experience in clinical research, data extraction, and regulatory navigation to ensure high-quality, compliant study records.

Competenze

  • 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.

Mansioni

  • Coordinate and manage data entry for oncology treatment trials.
  • Perform site initiation activities and ensure regulatory compliance.
  • Compile and maintain research patient records according to federal regulations and local policies.

Conoscenze

Previous experience with therapeutic <

Formazione

Bachelor's degree

Descrizione del lavoro

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

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

If time-limited, estimated duration of appointment

One of the best college towns and best places to live in the United States, Chapel Hill has diverse social, cultural, recreation and professional opportunities that span the campus and community.

University employees can choose from a wide range of professional training opportunities for career growth, skill development and lifelong learning and enjoy exclusive perks for numerous retail, restaurant and performing arts discounts, savings on local child care centers and special rates on select campus events. UNC -Chapel Hill offers full-time employees a comprehensive benefits package , paid leave, and a variety of health, life and retirement plans and additional programs that support a healthy work/life balance.

Primary Purpose of Organizational Unit

Our mission is to improve the health and well-being of North Carolinians and others whom we serve. We accomplish this by providing leadership and excellence in the interrelated areas of patient care, education and research.
Patient care: We promote health and provide superb clinical care while maintaining our strong tradition of reaching underserved populations and reducing health disparities across North Carolina and beyond.
Education: We prepare tomorrow`s healthcare professionals and biomedical researchers from all backgrounds by facilitating learning within innovative and integrated curricula and team-oriented interprofessional education to ensure a highly skilled workforce.
Research: We develop and support a rich array of outstanding health sciences research programs, centers and resources. We provide infrastructure and opportunities for collaboration among disciplines throughout and beyond our university to support outstanding research. We foster programs in the areas of basic, translational, mechanistic and population research.

Position Summary

The purpose of this position is to independently coordinate and manage data entry for oncology treatment trials, perform site initiation activities, and facilitate the comprehensive compilation of research patient records 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; or equivalent combination of training and experience. All degrees must be received from appropriately accredited institutions.

Management Preferences

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.

Required Licenses/Certifications

Special Physical/Mental Requirements

Campus Security Authority Responsibilities

Not Applicable.

Position/Schedule Requirements

Position/Schedule Requirements Clinic – UNCH or ACC, Evening work occasionally, Exposure to Bloodborne Pathogens, Exposure to Hazardous Materials, Overtime occasionally, Weekend work occasionally

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

Equal Opportunity Employer Statement

The University is an equal opportunity employer and welcomes all to apply without regard to age, color, gender, gender expression, gender identity, genetic information, national origin, race, religion, sex, or sexual orientation. We encourage all qualified applicants to apply, including protected veterans and individuals with disabilities.

Required Documents
  • Curriculum Vitae / Resume
  • Cover Letter
Optional Documents
  • List of References
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 Assistant position.
    • Bachelor's, Master's, and/or Doctorate in any field.
    • Associate's in any field and at least 2 years of experience.
    • Combination of post-high school education and experience to equal at least 4 years of related experience (ex: 1 year towards a degree and 3 years of experience).
    • High School diploma/GED and at least 4 years of related experience.
    • Did not complete high school but have a combination of high school education and experience to equal 8 years. (ex. 3 years of high school and 5 years of experience).
    • None of the above
  • * Do you have knowledge of GCP and ICH Guidelines?
    • Yes
    • No
  • * Do you have CCRP or CCRC Certification?
    • yes
    • no
  • * Describe your working knowledge and facility with information technology.

    (Open Ended Question)

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