Hybrid Clinical Research Data Coordinator II – Oncology

UAB Medicine

University (FL)

Híbrido

USD 45 000 - 74 000

Tempo integral

Há 7 dias
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Resumo da oferta

UAB Medicine seeks a Clinical Research Data Coordinator II for the O’Neal Comprehensive Cancer Center. You will design and maintain clinical data systems, ensure data integrity, and support data tracking and reporting across oncology trials.

Responsibilities include data entry, statistical summaries, and compliance with GCP/ICH guidelines. The role requires a related bachelor's degree with several years of experience and offers a hybrid work arrangement in a university cancer center setting.

Qualificações

  • Bachelor's degree in a related field and three years of related experience required.
  • Work experience may substitute for education requirement.
  • Experience with clinical trial data collection and GCP/ICH guidelines preferred.
  • Strong data entry and ability to read charts and extract information.

Responsabilidades

  • Design, implement and maintain clinical-based relational database management systems.
  • Ensure operation and maintenance of departmental systems for data organization, collection, retrieval, and reporting purposes.
  • Develop methods for tracking and reporting data and monitor incoming/outgoing data to ensure data integrity and compliance with applicable regulatory agency policy.
  • Research and collect information and enter data into established external data marts specified to clinical discipline and retrieve as necessary.
  • Perform a variety of statistical analyses and summarize results.
  • Performs other duties as assigned.

Conhecimentos

GCP knowledge
ICH guidelines
Clinical data entry
Communication skills

Formação académica

Bachelor's degree in a related field

Descrição da oferta de emprego

UAB Medicine seeks a Clinical Research Data Coordinator II for the O’Neal Comprehensive Cancer Center. You will design and maintain clinical data systems, ensure data integrity, and support data tracking and reporting across oncology trials.

Responsibilities include data entry, statistical summaries, and compliance with GCP/ICH guidelines. The role requires a related bachelor's degree with several years of experience and offers a hybrid work arrangement in a university cancer center setting.

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