Senior Assistant Study Coordinator

PeopleAdmin, Inc.

Chapel Hill (NC)

On-site

USD 42,000 - 64,000

Full time

18 hours ago
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Job summary

University of North Carolina at Chapel Hill's LCCC Cellular Therapy Program is seeking aClinical Data Management support for early-phase adult and pediatric cellular and gene therapy trials. You will ensure data collection aligns with GCP/ICH and institutional policies, handling abstraction, entry, and quality checks.

The role requires a Bachelor’s degree with experience in data management and oncology trials, working within a collaborative, regulated research environment.

Qualifications

  • Bachelor’s degree or equivalent combination of training and experience.
  • Experience in clinical data management and data quality assurance.
  • Familiarity with oncology clinical trials and regulatory guidelines.

Responsibilities

  • Abstract and review patient data for trials and reconcile discrepancies.
  • Enter data and perform quality control within EDC systems.
  • Serve as primary contact for data entry and coordination with study teams.

Skills

Clinical data management
Data abstraction
Query resolution

Education

Bachelor’s degree

Tools

EDC systems

Job description

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

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

If time-limited, estimated duration of appointment

This position is not eligible for H‑1B sponsorship.

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

UNC LCCC Cellular Therapy Program (https://unclineberger.org/cellular-immunotherapy/) is one of the select few academic centers in the United States with the scientific, technical and clinical capabilities to identify new tumor targets and develop and infuse novel CAR -T immunotherapy. The purpose of this position is to provide clinical data management support for the program’s complex, early‑phase adult and pediatric cellular and gene therapy clinical trials and to ensure that clinical data management activities are conducted according to federal regulations, Good Clinical Practice, and local and institutional policies. This position is responsible to clinical data abstraction and review, query resolution and reconciliation to support the delivery of clinical data. This position will be responsible for data entry activities, quality control review, identification, and documentation of data problems during EDC tracking and maintenance and serve as the primary contact for data entry activities for the program.

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
  • Clinical trial experience in oncology.
  • Previous experience with early‑phase therapeutic clinical research involving drugs and/or devices.
  • Experience navigating medical records and data extraction.
  • Research Certification – SOCRA / ACRP
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
  • 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
  • * Please describe your experience with oncology clinical trials.

    (Open Ended Question)

  • * Please describe your experience with data query and resolution.

    (Open Ended Question)

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