Clinical Research Coordinator (Hybrid)

Description

• Responsible for protocol compliance- making sure things are done in the correct timeframe.
• Work with clinic staff to make and schedule appointments, for example EKG’s or vitals.
• Collaborating with clinical folks that get insurance authorizations.
• Most of the time is spent in clinic- seeing patients with the doctor, go to patient visits, make sure the questionnaires are completed and research procedures outside the clinical norms are done.
• Interacting with nursing staff, MA’s.
• Responsible to screen, consent and enroll patients on an oncology trial and follow that patient through the course of therapy.

Requirements

• If someone had Phase I experience they could possibly run with Solid Tumor Oncology studies.
• The specialty could be Hematology Oncology, Breast Oncology, GU Oncology and GI Oncology.

Benefits

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

Training + Development

Interview process

Visa Sponsorship

Security clearance