Clinical Research Coordinator: Lead Patient Trials

The US Oncology Network; Annapolis (MD); On-site; USD 52,000 - 89,000; Full time

Job summary

The US Oncology Network is seeking a mid‑level Research Coordinator II to recruit, screen, consent, and enroll patients in clinical trials. You will coordinate visits, ensure protocol compliance, and support staff training across our Maryland/DC network.

Responsibilities include data collection, billing guidance, and ensuring quality through SOPs and GCP adherence while collaborating with physicians and study leaders.

Qualifications

• Associate’s degree in a clinical or scientific discipline required; Bachelor’s degree preferred.
• Minimum three years of experience in a clinical or scientific field.
• SoCRA or ACRP certification preferred.

Responsibilities

• Screen potential participants for protocol eligibility and present trial concepts to participants.
• Coordinate participant care to ensure protocol compliance and oversee orders and sample shipments.
• Document changes in condition, adverse events, and concomitant medications; collect data for study records.

Skills

Communication

Organization

Multitasking

Time management

Interpersonal skills

Attention to detail

Adaptability

Education

Associate degree

Bachelor’s degree preferred

Tools

Microsoft Office

Job description

The US Oncology Network is seeking a mid‑level Research Coordinator II to recruit, screen, consent, and enroll patients in clinical trials. You will coordinate visits, ensure protocol compliance, and support staff training across our Maryland/DC network.

Responsibilities include data collection, billing guidance, and ensuring quality through SOPs and GCP adherence while collaborating with physicians and study leaders.