Job Description

Clinical Research Associate role at ICON Strategic Solutions supporting multiple clinical trials across therapeutic areas with a focus on site selection and activation. The position involves collaborating with operations teams, conducting site qualification visits, and managing regulatory compliance in the Nashville, Tennessee area.

Responsibilities

• Identify, select, and activate clinical trial sites according to project timelines and requirements
• Conduct Site Qualification Visits to assess site eligibility for clinical studies
• Coordinate collection of regulatory approvals, contracts, and essential documentation for site activation
• Serve as primary contact for sites, study teams, and stakeholders throughout start-up process
• Monitor and report on key performance indicators related to site selection and start-up timelines

Requirements

• Bachelor's degree in Biological Sciences, R.N., or equivalent
• 2-3 years of pharmaceutical clinical trial monitoring experience
• 1-3 years of cross-therapeutic area clinical trial monitoring
• Knowledge of ICH-GCP guidelines and local regulatory requirements
• Proficiency with clinical trial management systems (CTMS, EDC, eTMF, IWRS)
• Strong communication and site management skills
• Legal authorization to work in the United States

Compensation: Competitive base salary and performance related incentives

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