Clinical Research Coordinator

Job Summary

Managing clinical trial protocols, the full-time Research Coordinator will recruit and screen patients, obtain informed consent, and coordinate study activities in a hybrid work environment.

Key responsibilities

• Determines protocol-related needs and manages research funds
• Recruits and screens potential patients, providing education on trial participation
• Prepares and submits Institutional Review Board (IRB) paperwork and maintains regulatory documents

Required qualifications

• Bachelor's Degree and research experience required; Master's Degree preferred
• Phlebotomy certification or venipuncture skills preferred
• BLS HCP certification from AHA preferred
• Certification in clinical research (SoCRA, ACRP) preferred