Clinical Research Coordinator II (Oncology)

Location: Frederick or Germantown, Maryland; full-time, on-site, Monday through Friday

Salary: $58,798–$77,435 per year

Company

hirify.global supports Maryland Oncology Hematology in delivering cancer care and conducting clinical research across Maryland and Washington, DC.

What you will do

• Screen patients for clinical trial eligibility, present trial information, support informed consent, and enroll participants.
• Coordinate patient visits and care according to protocol requirements, including investigational drug accountability and specimen shipments.
• Review patient condition changes, adverse events, medications, treatment response, and protocol compliance with physicians and care providers.
• Prepare protocol worksheets, adverse event reports, institutional review board documents, and continuing review reports.
• Maintain regulatory documentation, support monitoring and audit visits, and interact with study monitors and auditors.
• Compile protocol activity, accrual, data-entry compliance, billing, and research financial information.

Requirements

• Associate's degree in a clinical or scientific discipline required; bachelor's degree preferred.
• At least three years of experience in a clinical or scientific discipline required, preferably in oncology.
• Experience with Microsoft Office and strong communication, organization, multitasking, time-management, interpersonal, and attention-to-detail skills.
• Experience in patient-facing roles, with a professional and empathetic approach to care.
• Ability to work independently, manage priorities, and perform basic clinical assessments in a fast-paced environment.
• Hazmat and/or IATA training is required for applicable specimen-shipping duties.

Nice to have

• Bachelor's degree in a clinical or scientific discipline.
• SoCRA or ACRP certification.
• Experience working with physicians or in clinical research.

Culture & Benefits

• Supportive clinical research environment focused on patients, physicians, and colleagues.
• Participation in staff education, training, process improvement, and quality initiatives.
• Traditional office and oncology/hematology clinic environment.
• Work includes extensive computer use, standing and walking, and occasional lifting of items up to 40 pounds.