Clinical Research Associate

JOB DESCRIPTION

What You’ll Do:

• Lead and manage clinical sites throughout the trial lifecycle—from site identification to close-out.
• Monitor clinical data to ensure quality, accuracy, and compliance with FDA, ICH, SOPs, and protocols.
• Collaborate on clinical trial plans, including timelines, budgets, and regulatory documentation.
• Track study performance and KPIs to ensure projects are delivered on time and within scope.
• Resolve study challenges with proactive, solution-oriented thinking.

What You’ll Need:

• Bachelor’s degree with 5+ years of relevant experience, or a Master’s degree with 3+ years.
• Proven experience managing and monitoring clinical study sites.
• Strong knowledge of clinical trial regulations and best practices.

Preferred Experience:

• Background in IVD product development, particularly in molecular diagnostics, oncology, or infectious disease.
• Familiarity with laboratory automation and biological data systems.
• Solid understanding of medical terminology and clinical lab operations.