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Senior Study Manager, Immunology

Merck
September 10, 2026
Full-time
On-site
North Wales, PA
Clinical Research and Development
Role: Lead operational planning and execution of clinical trials within the Tulisokibart program, serving as a trial team lead and managing study activities across multiple stakeholders. Responsibilities: oversee feasibility, trial timeline management, risk mitigation, vendor/partner coordination, and study deliverables such as data management, site selection, and study close-out. Requirements: Bachelor's degree with 5+ years or Master's with 3+ years in pharmaceutical/clinical development, project management, or medical fields; PhD/PharmD preferred. Experience in global clinical trials, especially in immunology, autoimmune, dermatology, or gastroenterology, is highly desirable. Skills: strong project management, GCP/ICH knowledge, stakeholder influence, leadership, problem-solving, and excellent communication. HighValue: clinical trial leadership, immunology/autoimmune indications, global trial experience, vendor management, cross-functional collaboration. WorkSetup: primarily on-site with 10% travel.