Associate Director, Clinical Operations

Manage global clinical studies for Tessera’s genetic medicine programmes, from trial planning through close-out. Responsibilities include site and vendor selection, study budgets, recruitment planning, clinical documentation and review of trial data quality. The associate director leads cross-functional study teams and works with investigators and external research organisations. The position is based in Somerville, Massachusetts.

Bachelor’s degree in a relevant scientific or healthcare subject, at least eight years in clinical operations and four as a clinical trial manager. Requires global trial delivery, vendor oversight and ICH-GCP knowledge. Experience with rare diseases or gene therapy is strongly preferred.