Oncology Clinical Research Coordinator

US Oncology Inc.

Fairfax (VA)

Presencial

USD 50.000 - 80.000

Jornada completa

Hace 2 días
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Descripción de la vacante

Virginia Cancer Specialists in Fairfax seeks a Full Time Clinical Research Coordinator to coordinate screening, enrollment, and maintenance of patients on clinical trials, ensuring protocol compliance and accurate documentation in collaboration with physicians.

The ideal candidate holds an Associate's degree in a clinical or scientific field, preferably with oncology experience; Bachelor's preferred. SOCRA or ACRP certification is a plus, with strong communication and organizational skills.

Formación

  • Associate's degree in a clinical or scientific discipline required; Bachelor's degree preferred.
  • Minimum three years of experience in a clinical or scientific related discipline required, preferably in oncology.
  • SOCRA or ACRP certification preferred.
  • Experience with Microsoft Office; strong communication and organizational skills.

Responsabilidades

  • Coordinate screening, enrollment, and maintenance of patients on clinical trials.
  • Ensure protocol compliance and participate in informed consent processes.
  • Assist with patient assessments, adverse events, and data entry.
  • Maintain investigational drug accountability and educate staff and patients.
  • Assist with billing information submission and study recruitment strategies.
  • Ensure compliance with US Oncology SOPs, GCP, and applicable regulations.
  • Collaborate with physicians and research team; participate in training.

Conocimientos

Communication skills
Organizational skills
Time management
Attention to detail
Multi-tasking
Interpersonal skills

Educación

Associate's degree
Bachelor's degree preferred

Herramientas

Microsoft Office

Descripción del empleo

Virginia Cancer Specialists in Fairfax seeks a Full Time Clinical Research Coordinator to coordinate screening, enrollment, and maintenance of patients on clinical trials, ensuring protocol compliance and accurate documentation in collaboration with physicians.

The ideal candidate holds an Associate's degree in a clinical or scientific field, preferably with oncology experience; Bachelor's preferred. SOCRA or ACRP certification is a plus, with strong communication and organizational skills.

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