The Senior Accountant, Commercial Finance reports directly to the Manager, Commercial Finance and works closely with other functions, including FP&A and Commercial business teams to ensure a timely and complete close and forecasting process. The Senior Accountant will be a key individual contributor, whose principal responsibilities will be the preparation of monthly accru

This individual will support quality control activities related to custom raw material manufacture for RNA and AAV gene therapy products conducted both internally and at various contract manufacturing organization (CMO) sites. The work involves reviewing data gathered from routine testing as well as from validations and qualifications. The scope will also include generatin

The person in this position will be working with a cross functional team as the project biostatistician responsible for statistical activities at the compound level or study level for one or more Gene therapy programs. It is an excellent opportunity to work at the forefront of precision genetic medicine, making an impact to the development of transformative therapies that

The Real World Evidence (RWE) Epidemiology Contractor RWE will provide leadership for scientific prospective and retrospective activities in the RWE team supporting Sarepta. The Real World Evidence (RWE) Epidemiology Contractor RWE will function in a company matrix team environment interacting with several key stakeholder groups including; Clinical Development, Pharmacovig

The Director, Clinical Development is responsible for leading a clinical sciences team responsible for advancement of Sarepta's clinical stage programs. The individual is responsible for defining strategic priorities for the program and integrating cross functional input in order to develop and execute the clinical development plan. The individual may be called upon to rep

This position will work with the central scheduling manager with retrospective and active data entry to support Non clinical studies within an electronic database. Additionally, this position will support scheduling in vivo activities as needed to ensure a timely proposed schedule for non clinical study directors using project management software. The contract research ass

The Senior Research Associate will report to the Associate Director, Drug Product Development. The position will focus mainly on internal development and support external activities for performing sterile injectable drug product development activities for Sarepta's Gene Therapy, PMO, and PPMO programs. This position will work closely with Drug Product Operations, QA/QC, an

The Senior Manager of Technical Operations will help drive the development of Sarepta's Gene Therapy and RNA Therapeutics platforms. Working within the broader Technical Operations department, he/she will be responsible for managing key business operations projects with particular focus on strategic commercial/clinical supply agreements and process development contract neg

The Senior Specialist, International Business Unit is responsible for implementing and executing operational tasks reporting into the SVP, International Business Unit. This role fulfills administrative duties and supports senior leaders across the function with maintaining the general, day to day operations of the broader team. There will also be opportunities for this per

The Associate Director, Commercial Diagnostics & Bioinformatics reports into the Executive Director, Commercial Diagnostics and plays a key role in driving the strategic vision and objectives to make Sarepta a recognized leader in precision genetic medicine for rare diseases. The Associate Director, Commercial Diagnostics analyzes genetic diagnostic data to provide insight

This individual will support routine testing conducted at Sarepta Andover laboratory charged with the execution of Nucleic Acids Testing (release and stability) related to Sarepta' s Gene Therapy pipeline conducted internally. The individual will conduct GMP QC release and stability testing using state of art Quantitative Polymerase Chain Reaction, qPCR, Droplet Digital PC

This position will be responsible and accountable for leading the Global Program Team (GPT) to create and execute an integrated development strategy which coherently integrates the clinical, non clinical, regulatory, medical affairs, manufacturing, commercial, and market access plans to support successful submissions, approvals, launch, and life cycle activities. It will c

The Associate Director of Finance Inventory and Manufacturing Operations will be responsible for managing the execution of processes aimed at delivering performance based analytics within the Technical Operations organization. Key duties include managing the product costing process to support strategic business planning, standard costing, and the annual business planning c

This individual will support method development, validation, and quality control activities conducted at Sarepta Andover in compliance with cGMP regulations. The individual will devise, troubleshoot, and validate cell based assays to assess the critical quality attributes of AAV gene therapy products including potency and infectivity. This role would facilitate activities

The Finished Goods Lead of Quality Assurance Operations would perform the person in plant oversight for Sarepta quality operations (for clinical and commercial) related to Gene Therapy CMOs. This person will oversee on site batch record review with on the floor support at the Philadelphia facility and perform product disposition activities. They would provide oversight of