Hybrid: Head & Neck Clinical Research Data Coordinator

MD Anderson Cancer Center

Houston (TX)

Hybrid

USD 44.000 - 66.000

Vollzeit

Vor 5 Tagen
Sei unter den ersten Bewerbenden

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Benefits dieser Stelle

Medical coverage from day one
Paid time off and holidays
Tuition assistance

Zusammenfassung

MD Anderson Cancer Center is seeking a Clinical Research Data Coordinator to support head and neck clinical studies. You will ensure accurate data collection, manage data via OnCore, OneIRB, and Epic, and collaborate with investigators and healthcare teams to advance trials.

The position emphasizes data integrity, protocol compliance, and timely reporting. A Bachelor’s degree is preferred, with experience in clinical research and strong organizational skills.

Qualifikationen

  • Requires High School Diploma or Equivalent; Bachelor's preferred.
  • Experience in patient-facing roles with strong communication and interpersonal skills.
  • Knowledge of research protocols, data collection methods, and human subjects research processes.
  • Proficiency with data management software, electronic medical records systems, and clinical research databases.

Aufgaben

  • Abstract and collect patient data from health records and source documents.
  • Ensure data quality through tracking, QA reviews, data entry, and query generation.
  • Assist with database coordination and maintenance for institutional studies.
  • Develop systems to control data flow and track non-database data.
  • Provide data for study progress, safety reports, IRB reviews, and reporting.

Kenntnisse

Communication
Interpersonal skills
Data management

Ausbildung

Bachelor's Degree
High School Diploma or Equivalent

Tools

OnCore
OneIRB
Epic

Jobbeschreibung

MD Anderson Cancer Center is seeking a Clinical Research Data Coordinator to support head and neck clinical studies. You will ensure accurate data collection, manage data via OnCore, OneIRB, and Epic, and collaborate with investigators and healthcare teams to advance trials.

The position emphasizes data integrity, protocol compliance, and timely reporting. A Bachelor’s degree is preferred, with experience in clinical research and strong organizational skills.

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