Clinical Trials Coordinator — Oncology Focus

City of Hope; Chevy Chase (MD); On-site; USD 55,000 - 75,000; Full time

Job summary

Retina Group of Washington, a PRISM Vision Group Partner Practice, seeks a Clinical Research Coordinator in Chevy Chase, MD to support study coordination and data collection. The role involves screening patients for eligibility, coordinating informed consent, and enrolling participants in oncology-focused trials.

Responsibilities include drug accountability, regulatory documentation, and collaboration with physicians to ensure protocol compliance while maintaining accurate data and billing

Qualifications

• Associate's degree in a clinical or scientific discipline required; Bachelor's preferred.
• Minimum five years of experience in a clinical or scientific field, preferably oncology.
• SoCRA or ACRP certification preferred.
• Experience in Microsoft Office; experience working with physicians is preferred.
• Strong communication, organization, and attention to detail; ability to work in fast-paced environment.

Responsibilities

• Screens potential patients for protocol eligibility.
• Present trial concepts, obtain informed consent, and enroll patients.
• Disburse investigational drug and maintain accountability.
• Prepare and review protocol documents and adverse events.
• Collaborate with physicians to ensure protocol compliance and data collection.
• Support billing review and submission as needed.

Skills

Communication skills

Organizational skills

Multi-tasking

Time management

Interpersonal skills

Attention to detail

Education

Associate's degree in clinical or scientific discipline

Bachelor's degree preferred

Tools

Microsoft Office

Job description

Retina Group of Washington, a PRISM Vision Group Partner Practice, seeks a Clinical Research Coordinator in Chevy Chase, MD to support study coordination and data collection. The role involves screening patients for eligibility, coordinating informed consent, and enrolling participants in oncology-focused trials.

Responsibilities include drug accountability, regulatory documentation, and collaboration with physicians to ensure protocol compliance while maintaining accurate data and billing