Senior Clinical Research Coordinator - Full Time - 1st Shift

Dayton Childrens Hospital

Dayton (OH)

Presencial

USD 60.000 - 80.000

Jornada completa

Hace 7 días
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Descripción de la vacante

Dayton Children's Hospital in Dayton, OH seeks a Senior Clinical Research Coordinator for the Neurology department. The role operates under the Clinical Research Supervisor/Manager and a Principal Investigator, adhering to ICH-GCP guidelines.

Lead assigned studies, ensure quality, and oversee feasibility, screening, enrollment, and study visits. Responsibilities include CRF completion, source document maintenance, and ensuring site quality; must ensure participant safety and regulatory

Formación

  • Bachelor's degree in health sciences or a related field.
  • Strong organizational skills and ability to work independently.
  • Experience/comfort with Electronic Data Capture (EDC) systems.

Responsabilidades

  • Lead site feasibility and preparation for assigned studies.
  • Screening and recruitment of patients, enrollment and conduct of study visits.
  • Complete and ensure quality of case report forms (CRFs) and source documents.
  • Maintain source documents and ensure site quality throughout the study.
  • Ensure participant safety and compliance with applicable regulations.

Conocimientos

EDC systems

Educación

Bachelor's degree in health sciences or related field

Descripción del empleo

Facility

Dayton Children's - Main Campus

Department

Neurology

Schedule

Full time Hours: 40

Job Details

The Senior Clinical Research Coordinator will perform clinical research activities under minimal direction of the Clinical Research Supervisor/Manager and a Principal Investigator (PI), while adhering to International Conference on Harmonization (ICH) and Good Clinical Practice (GCP) guidelines. The Coordinator will play a lead role in assigned studies and will be critical to ensuring all studies are conducted to a high standard of quality. The Coordinator will perform tasks including, but not limited to, site feasibility and preparation, patient screening and recruitment, patient enrollment, conducting study visits, completing and ensuring the quality of case report forms, maintaining source documents, and ensuring site quality.

All clinical research activities must be conducted in accordance with applicable federal and state regulations. Most importantly, the Senior Clinical Research Coordinator will ensure the safety and well-being of all study participants throughout all study activities.

Required Qualifications
  • Bachelor's degree in health sciences or a related field
  • Strong organizational skills, proficiency in Electronic Data Capture (EDC) systems, and ability to work independently.
Preferred Qualifications
  • 3+ years of experience in clinical research Department Specific Job Details:
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