The Associate Director will develop and implement marketing strategies for ELEVIDYS, collaborating with cross-functional teams and managing promotional materials to optimize brand performance and engage healthcare providers.

Coordinate business operations by managing contracts, purchase orders, and supporting budgeting processes to improve efficiency across departments.

The Director will lead CMC project management activities for gene therapy and RNA portfolio, ensuring successful advancement through collaboration with cross-functional teams.

The Director of Regulatory Labeling is responsible for leading labeling strategy, developing documents, and ensuring compliance with regulations. They oversee cross-functional teams and contribute to company goals while advancing product labeling processes.

The Director of International Business will enhance patient access to treatments by managing supply chains, partnerships, and compliance with international regulations.

The Safety Scientist at Sarepta will support risk management and safety reporting in the Global Pharmacovigilance department, evaluating safety data for drugs, participating in discussions, and contributing to safety evaluations and governance activities.

The Scientist II role involves preparing nonclinical regulatory documents, ensuring data quality, collaborating with teams, and assisting with statistical analyses for IND submissions.

Lead Translational Pharmacology team overseeing nonclinical pharmacology activities, including modeling, study design, regulatory strategies, and team management for genetic therapies.

The Associate Director of Legal Counsel provides legal advice on employment-related matters, partners with HR, advises on compliance, and presents to leadership.

The Logistics Coordinator manages shipment processes, ensures accuracy, handles inventory, inspects shipments, and supports operations within regulated environments.

The Lead Process Engineer will support gene therapy programs, manage projects, ensure compliance with regulatory standards, and improve processes for production efficiency.

The Senior Director leads a Quality Control testing team, ensuring completion of lot release, overseeing analytical testing, mentoring staff, and engaging with regulatory agencies.

Oversee and manage all logistics and trade compliance activities, ensuring adherence to regulations and operational efficiency. Lead a team, develop strategies, manage budgets, and drive continuous improvement.

Assist in executing preclinical research studies, prepare materials, maintain reagents, support GLP/GCP drug development, and troubleshoot technical challenges.

The R&D Business Systems Intern will support R&D systems management, troubleshooting, systems integration, and participate in project management in a hybrid role.

The Senior Manager analyzes genetic diagnostic data to guide commercial activities, develop data strategies, and ensure data integrity. This role involves collaboration with stakeholders, data visualization, and managing data pipelines.

The HR Systems Analyst will support and optimize the Workday system, analyze employee data, and provide technical support to HR operations.

As a Gene Editing Intern, you will conduct in vitro experiments, develop disease models, and implement gene therapy strategies under supervision while maintaining lab compliance and documentation.

The Director, Clinical Operations Program Lead will oversee early phase studies, ensuring they are completed on time and within budget, while leading a high-quality team and collaborating cross-functionally.

The Senior Director of Strategy & Operations leads strategic Technical Operations initiatives, focusing on growth, operational digitization, and collaboration within various departments to optimize investments and decisions.