Sarepta Therapeutics

HQ
Cambridge
Total Offices: 4
1,464 Total Employees

Sarepta Therapeutics Benefits Overview

Compensation + Benefits

Offers 401(K)

Offers life insurance

Offers disability insurance

Offers accidental death & dismemberment insurance

Offers company equity

Offers performance bonuses

Offers employee stock purchase plan

Offers dental insurance

Offers health insurance

Offers mental health benefits

Offers Flexible Spending Account (FSA)

Offers vision insurance

Offers Health Savings Account (HSA)

Provides family medical leave

Offers generous parental leave

Company Culture

Provides commuter benefits

Provides free snacks and drinks

Utilizes a flexible work schedule

Offers a remote work program

Offers diversity-based Employee Resource Groups

Work-Life Balance + Wellbeing

Offers company-sponsored outings

Offers gym membership

Offers an Employee Assistance Program (EAP)

Offers generous PTO

Provides paid sick days

Provides paid holidays

Provides bereavement leave

Career Growth + Development

Provides customized development tracks

Provides tuition assistance

Biotech
Promotes Sarepta’s neuromuscular therapies to healthcare providers across an assigned U.S. territory. The role develops referral networks, educates providers on Duchenne muscular dystrophy treatments, genetic testing, antibody assays, access, and reimbursement, and drives enrollment and sales goals. Responsibilities include consultative selling, account planning, weekly in-person provider meetings, cross-functional collaboration, regulatory compliance, and maintaining advanced knowledge of the rare-disease treatment environment. The position requires living within the assigned geography and traveling up to 70%.
2 Hours AgoSaved
Remote or Hybrid
United States
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Lead translational biomarker strategy and implementation across nonclinical and clinical programs (emphasis on siRNA). Oversee assay development/validation, CRO/vendor management, data analysis of large omics datasets, regulatory writing, and cross-functional collaboration to support program decision-making and data dissemination.
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Remote or Hybrid
2 Locations
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Leads statistical strategy and execution for clinical trials from protocol design through analysis, reporting, and regulatory submission. Serves as study and future program statistical lead, guiding adaptive trial design, pivotal analyses, integrated analyses, and regulatory interactions. Partners cross-functionally, oversees CROs and programmers, independently develops analyses in R or SAS, and mentors statisticians and programmers while helping build the Biostatistics function.