Senior Clinical Trial Associate

Role: Senior Clinical Trial Associate supporting global clinical trial operations in biopharma, focusing on neuromuscular disease programs. Responsibilities include assisting in study planning, execution, and closeout across all trial phases, coordinating communication among internal teams, CROs, and vendors, tracking operational metrics, ensuring regulatory and documentation compliance, and supporting inspection readiness. The role emphasizes process improvement, accurate documentation, and stakeholder engagement. Requirements: Bachelor's in life sciences or related field; 3+ years of clinical operations or drug development experience, preferably in sponsor settings with global/multi-site trials; knowledge of GCP, regulatory standards, TMF management, and trial tracking systems; proficiency with Microsoft Office and clinical tools; ability to work independently and collaboratively. Preferred qualifications include experience across cross-functional teams such as Clinical Operations, Regulatory, Data Management, and Quality. High-value specifics include focus on neuromuscular diseases, clinical trial phases, global trial support, inspection preparedness, and travel (~5%). The position is based in Waltham, MA, with responsibilities centered on supporting the clinical development portfolio of DMD, DM1, FSHD, Pompe, and other genetic neuromuscular conditions.