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Associate Director, Clinical Study Quality Lead (Hybrid)

Vertex PharmaceuticalsBoston, MA

$160,600–240,800/yr

Posted Oct 16, 2026

What you’d do

Serves as a GCP subject matter expert providing risk-based quality compliance oversight of clinical studies in assigned disease areas, consulting on regulations and quality systems and partnering with study teams on risk mitigation. Full time hybrid role in Boston, MA. Found on the employer's careers page on Oct 17, 2026. Apply through the link.

You’ll need

  • Bachelor's in scientific or allied health field
  • 8+ years relevant work experience
  • In-depth knowledge of ICH-GCP guidelines
  • Knowledge of FDA, EMA, MHRA regulations

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