Advanced Oncology Clinical Research Coordinator (Remote)

American Oncology Partners, PA

Fredericksburg (VA)

Presencial

USD 2.893.000 - 4.896.000

Jornada completa

Hace 7 días
Sé de los primeros/as/es en solicitar esta vacante
Generador de candidaturas

Una candidatura completa en un minuto — currículum y carta de presentación personalizados, listos para enviar.

Supera los filtros ATS

Ventajas ofrecidas por este puesto de trabajo

Health insurance
401k with match
Paid time off

Descripción de la vacante

American Oncology Network AON seeks an experienced Clinical Research Coordinator II (non-RN) to independently manage complex oncology trials under PI supervision. You will oversee protocol adherence, regulatory compliance, and patient coordination across multiple trials with a strong emphasis on data integrity and safety reporting.

The role requires 2–5 years oncology research experience, familiarity with GCP/ICH guidelines, and proficiency in EMR/EDC systems.

Formación

  • Education: High school required. Some college preferred; bachelor’s degree preferred.
  • Licensed Practical Nurse (LPN) may be required per role.
  • 2–5 years oncology research/related medical science experience.

Responsabilidades

  • Coordinate care for patients on clinical research protocols per GCP/ICH FDA guidelines.
  • Manage data integrity and documentation for multiple trials.
  • Support regulatory submissions and site IRB/IEC processes.

Conocimientos

Analytical thinking
Regulatory knowledge
Communication skills
Team collaboration
Time management

Educación

High school diploma
Some college
Bachelor’s degree preferred
Licensed Practical Nurse (LPN) required

Herramientas

MS Office (Word, Excel, PowerPoint, Outlook)
EMR
EDC systems
CTMS

Descripción del empleo

American Oncology Network AON seeks an experienced Clinical Research Coordinator II (non-RN) to independently manage complex oncology trials under PI supervision. You will oversee protocol adherence, regulatory compliance, and patient coordination across multiple trials with a strong emphasis on data integrity and safety reporting.

The role requires 2–5 years oncology research experience, familiarity with GCP/ICH guidelines, and proficiency in EMR/EDC systems.

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