Oncology Clinical Research Coordinator – Full Time

Virginia Cancer Specialists, P.C.; Fairfax (VA); On-site; USD 55,000 - 75,000; Full time

Job summary

Virginia Cancer Specialists, an affiliate of US Oncology, seeks a Full Time Clinical Research Coordinator for our Fairfax office. A Bachelor's degree in a clinical or scientific related discipline is desired, and oncology experience is preferred.

The coordinator screens, enrolls, and maintains patients on trials, ensures protocol compliance, participates in consent, and maintains accurate data. It requires excellent communication, organization, multitasking, and attention to detail in a

Qualifications

• Bachelor's degree in a clinical or scientific related discipline required, Bachelor's degree preferred.
• SOCRA or ACRP certification preferred.
• Excellent communication and organizational skills; ability to multi-task.

Responsibilities

• Collaborates with physicians and providers to screen potential patients for eligibility.
• Presents trial concepts, participates in informed consent, and enrolls patients.
• Coordinates patient care per protocol; dispenses investigational drug and teaches administration.
• Maintains investigational drug accountability and documents findings; monitors adverse events.
• Reviews protocol billing guides and submits billing information to appropriate personnel.
• Assists with recruitment goals and strategies to retain participants in trials.
• Provides clinical services as required and assists with regulatory documents and staff education.
• Supports scheduling monitoring and audits; communicates with monitors and physicians.

Skills

Communication

Organization

Multitasking

Time management

Attention to detail

Interpersonal skills

Education

Associate's degree in clinical/science

Bachelor's degree preferred

Job description

Virginia Cancer Specialists, an affiliate of US Oncology, seeks a Full Time Clinical Research Coordinator for our Fairfax office. A Bachelor's degree in a clinical or scientific related discipline is desired, and oncology experience is preferred.

The coordinator screens, enrolls, and maintains patients on trials, ensures protocol compliance, participates in consent, and maintains accurate data. It requires excellent communication, organization, multitasking, and attention to detail in a