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

Sarepta Therapeutics is seeking a motivated facility dependent individual with histology and immunohistochemistry experience. The qualified candidate will provide laboratory support of day to day GLPs (Good Laboratory Practices) testing on muscle, nerve, and other types of tissue using complex prosecting and histology methods in accordance with the requirements of approved

The Duchenne Area Manager (DAM) is a performance driven individual contributor that promotes the safe and effective use of Sarepta Therapies to medical providers across their assigned territory. This role serves as part of a larger team that forge opportunities for newly approved classes of drugs to treat Duchenne Muscular Dystrophy, a rare life threatening pediatric disea

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

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

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 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

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

As a member of the Analytical Development group this position is responsible for performing GLP method validation and GLP analytical assay support for early stage research programs. The individual will collaborate with Early Research Process Development, Gene Therapy Research, and additional internal and external stakeholders to support nonclinical GLP studies. Primary Res

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

Sarepta Therapeutics is seeking a motivated facility dependent scientist with expertise in digital image analysis development, validation, execution, and reporting. The qualified candidate will provide scientific oversight into the development strategies and validation studies in alignment with current regulatory guidance for Bioanalytical Method Validation and relevant hi

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

This individual will be a member of the local quality team that supports preclinical and clinical gene therapy research functions. The candidate will have a clear understanding of the data capture process and will perform QC review of gene therapy research data under direct supervision. The candidate will assist with tracking, trending, and reporting results. The candidate

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