The Principal Scientist functions as a subject matter expert and has direct oversight to ensure successful implementation, execution, and completion of non clinical studies. The individual filling this position must have extensive Good Laboratory Practice (GLP) experience and must be able to influence best practices. The Study Director will assume the responsibility for th

The Associate Director, IT End User Services directs IT efforts for global help desk, desk side services, and inventory management for technology assets. In this position, you will oversee help desk support to ensure that the End User Services team is responding to user questions and problems, assist on site IT personnel to maintain laptos, desktops, peripherals, and telec

The Patient Service Specialist II (Contractor) supports Duchenne Muscular Dystrophy patients and families as a member of the Patient Services Team. Paired with a Case Manger(s), the Patient Service Specialist II supports the team through data updates to patient records, tracking case status, set up of new patient referrals and patient outreach. The Patient Service Speciali

The Associate Director, Nonclinical Quality will be responsible to provide direction to team members around prioritization of deliverables and to work with quality management in conjunction with Genetic Therapies Center of Excellence (GTCOE) and Translational Biology departments. The qualified candidate will serve as a Subject Matter Expert to ensure that activities perfor

The Director, Quality Operations within Research & Clinical Development Quality Assurance will be responsible for the oversight and support of the Sarepta Clinical Development and Real World Evidence portfolio. The qualified candidate will serve as a Subject Matter Expert to ensure that activities performed by Clinical Trial Teams are in compliance with regulatory requirem

The Senior Director, Global Market Access Strategy (GMAX) drives market access strategy for Sarepta's assets with influential leadership that represent the goals and priorities of the broader International Business Unit to cross functional teams such as the Global Product Team (GPT) or Customer Org Sub Team (CT). This role is responsible for developing market access and ev

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 Real World Evidence (RWE) lead provides clinical leadership for evidence generation activities, supporting the integration of RWE into Sarepta key strategic initiatives. The role functions in a company matrix team environment interacting with several key stakeholder groups including; Clinical Development, Pharmacovigilance, Regulatory Affairs, Quality Assurance, Manufa

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 Sr. Manager, GxP Training position is responsible to manage Sarepta's global GxP Training Program. The position will reside on site in the Andover, MA facility, reporting to the Director of Global Quality Systems. The position encompasses a variety of training management responsibilities, including maintaining a compliant GxP Training Program in accordance with US and

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 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

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 Manager, Data Governance & Analytics assists in leading a data driven approach to support key strategic initiatives that ensure the launch and commercial success of Sarepta's current platform and pipeline products. This position partners with several Customer teams to ensure effective and impactful leverage of analytics initiatives. This role partners with Field Analyt