Clinical Research Coordinator: Lead Patient‑Centric Trials

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

Job summary

Maryland Oncology Hematology is seeking a mid-level Clinical Research Coordinator II to recruit, screen, consent, and enroll patients in clinical trials across our Maryland/DC network. You will coordinate visits, ensure protocol compliance, and support education of clinic staff while upholding GCP and SOP standards.

The role emphasizes attention to detail, strong communication, and teamwork in a busy research environment.

Qualifications

• Associate's degree required; Bachelor's preferred.
• Minimum three years of clinical or scientific experience.
• SoCRA or ACRP certification preferred.

Responsibilities

• Screen and enroll participants for clinical trials per protocol.
• Coordinate participant care and ensure protocol compliance.
• Prepare documentation: worksheets, adverse event reports, IRB documents.
• Maintain regulatory files and assist with monitoring visits.
• Educate clinical staff and support data collection and reporting.

Skills

Excellent communication

Strong organizational abilities

Multitasking

Time management

Education

Associate's degree in clinical or scientific discipline

Bachelor's degree preferred

SoCRA or ACRP certification preferred

Tools

Microsoft Office

Job description

Maryland Oncology Hematology is seeking a mid-level Clinical Research Coordinator II to recruit, screen, consent, and enroll patients in clinical trials across our Maryland/DC network. You will coordinate visits, ensure protocol compliance, and support education of clinic staff while upholding GCP and SOP standards.

The role emphasizes attention to detail, strong communication, and teamwork in a busy research environment.