Hiring: Associate Director, Global Submission Management Company: Vertex Pharmaceuticals Location: Boston, MA Job Posted Time: 2026-09-11 11:47:33 Employment Type: Hybrid Target Skills & Keywords : Project Management, Stakeholder Management About the job Experience: •7+ years of experience in regulatory submission management, regulatory operations, or regulatory/clinical project management •People‑management experience preferred Required Skills: •Provides oversight for a defined portfolio of regulatory submissions, from planning through submission and closeout •Develops and maintains submission plans, timelines, and tracking across multiple programs •Ensures consistent application of submission management standards, tools, and processes •Partners with Global Regulatory Strategy, Regulatory CMC, Labeling, Publishing, and Advertising & Promotion to define submission scope, milestones, and deliverables •Coordinates cross‑functional activities to ensure submission completeness, quality, and compliance •Identifies, manages, and resolves operational risks affecting submission timelines or quality •Oversees preparation of submission status updates, issue logs, and portfolio‑level reporting •Supports workload planning and capacity management across the submission portfolio Qualifications: •Bachelor’s degree in Life Sciences, Regulatory Affairs, Project Management, or a related discipline Compensation: •$163,200 - $244,800 / year •Flexible work environment (work from home / hybrid options) •This role is eligible for an annual bonus and annual equity awards Interested candidates, please apply directly through the job posting on company's career page or try via AI auto apply on this platform. Don't miss this opportunity to join a forward-thinking team!