Clinical Research Coordinator

Description

• Screen newly diagnosed, progressed, or recurrent patients for trial eligibility and provide protocol-specific information to patients, physicians, and nurses.
• Ensure protocol compliance and coordinate follow-up procedures to assess treatment response and toxicity.
• Maintain accurate patient status in CTMS and EPIC within 24 hours of enrollment or status change.
• Collect and submit clinical trial data to NCI, industry sponsors, with high accuracy and timeliness.
• Complete case report forms (CRFs), including QOL surveys, radiologic scans, and staging tests, per protocol and sponsor requirements.
• Collaborate with physician investigators to identify, consent, screen, and enroll eligible patients into clinical trials.
• Attend tumor boards, clinics, and multidisciplinary meetings to identify potential trial candidates.
• Prepare and ship protocol-related specimens in compliance with OSHA guidelines.

Requirements

• Oncology experience is highly preferred.
• 2+ years of experience as a Clinical Research Coordinator.
• Experience with EPIC/Rave EDC is highly preferred.
• 4-year degree is required.

Benefits

• Medical, dental & vision
• Short and long-term disability
• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
• Transportation benefits
• Health Spending Account (HSA)
• Time Off/Leave (PTO, Vacation or Sick Leave)
• Employee Assistance Program
• Critical Illness, Accident, and Hospital
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)

Training + Development

Interview process

Visa Sponsorship

Security clearance