Clinical Research Coordinator II – Oncology Trials

American Oncology Network, Inc.; Fredericksburg, Northern (VA, KY); Hybrid; USD 29.000 - 50.000; Vollzeit

Zusammenfassung

American Oncology Network, Inc. seeks a Clinical Research Coordinator II (Non-RN) in Fredericksburg, VA to oversee complex Phase 1–3 trials with rigorous regulatory adherence.

You will manage protocol feasibility, subject eligibility, and informed consent discussions alongside PI supervision. Responsibilities include data accuracy, adverse event tracking, CRMS/EHR documentation, and study budget considerations.

Qualifikationen

• 2–5 years of oncology research/related medical science experience.
• Must understand GCP/ICH-FDA guidelines and be able to implement protocol procedures.
• Experience with multi-site or multi-cohort studies is a plus.
• Strong data management and regulatory documentation capabilities.

Aufgaben

• Coordinate care for patients on clinical research protocols per GCP/ICH-FDA guidelines.
• Review informed consent documents and discuss with subjects per SOPs.
• Maintain accurate trial records and manage investigational products per sponsor guidelines.
• Assist with budget development and ensure trial billing compliance.

Kenntnisse

Analytical thinking

Communication

Interpersonal skills

Time management

Self-management

Ausbildung

High school

Some college

Bachelor’s degree

Licensed Practical Nurse

Tools

EMR

EDC

CTMS

MS Office

Jobbeschreibung

American Oncology Network, Inc. seeks a Clinical Research Coordinator II (Non-RN) in Fredericksburg, VA to oversee complex Phase 1–3 trials with rigorous regulatory adherence.

You will manage protocol feasibility, subject eligibility, and informed consent discussions alongside PI supervision. Responsibilities include data accuracy, adverse event tracking, CRMS/EHR documentation, and study budget considerations.