Responsibilities

• Identify potential study participants through electronic medical records, physician referrals, and outreach campaigns.
• Educate patients about clinical trial participation, benefits, and expectations in a professional and compliant manner.
• Schedule patient visits and coordinate with study coordinators, investigators, and site staff.
• Maintain accurate and confidential documentation of recruitment and pre-screening activities per HIPAA and FDA regulations.
• Collaborate with physician offices, primary care clinics, and specialists to generate referrals.
• Meet recruitment goals and report weekly progress to the site manager or project lead.
• Ensure all recruitment practices align with Good Clinical Practice (GCP) guidelines and company SOPs.

Education

• Associate (required)

Language

• English (required)