Pediatric Human Subjects Research Specialist

University of Rochester

United States

Presencial

USD 30 000 - 42 000

Tempo integral

Há 8 dias

Uma candidatura completa num minuto

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Resumo da oferta

The University of Rochester seeks a detail-oriented Research Coordinator to support pediatric allergy and immunology human subject studies. You will coordinate administrative tasks, manage biospecimen processing, and assist in recruitment and screening while ensuring compliance with IRB and regulatory standards.

Experience with REDCap, data entry, and strong organizational skills are preferred. This on-site role offers the chance to contribute to cutting-edge clinical research in a collaborative

Qualificações

  • Bachelor's degree required or Associate's degree with 6 months in the Human Subject Research Coordinator Trainee program or equivalent combo of education and experience.
  • Prior phlebotomy experience preferred.
  • Word processing and data analysis software preferred.
  • Excellent organizational skills preferred.

Responsabilidades

  • Coordinates activities for human subject research in pediatric allergy and immunology.
  • Supports administrative and logistical details to initiate and conduct studies, including presenting protocol and recruitment materials.
  • Prepares sample kit distribution and processing of biospecimens.
  • Assists in recruitment and screening activities and reviews patient databases for eligibility.
  • Participates in developing recruitment strategies and may conduct telephone screens.

Conhecimentos

Coordination
Data entry
IRB liaison
GCP knowledge
Phlebotomy
Documentation

Formação académica

Bachelor's degree

Ferramentas

REDCap
Microsoft Word
Excel

Descrição da oferta de emprego

The University of Rochester seeks a detail-oriented Research Coordinator to support pediatric allergy and immunology human subject studies. You will coordinate administrative tasks, manage biospecimen processing, and assist in recruitment and screening while ensuring compliance with IRB and regulatory standards.

Experience with REDCap, data entry, and strong organizational skills are preferred. This on-site role offers the chance to contribute to cutting-edge clinical research in a collaborative

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