Sarepta Therapeutics Visa Sponsorship Jobs USA
Sarepta Therapeutics is a clinical-stage biopharmaceutical company focused on genetic medicine, best known for its work in rare neuromuscular diseases. It has an active visa sponsorship program, supporting H-1B visa, Green Card, F-1 OPT, and TN visa candidates across scientific and corporate functions.
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Get Access To All JobsWhy Sarepta? Why Now?
The promise of genetic medicine has arrived, and Sarepta is at the forefront. We hold a leadership position in Duchenne muscular dystrophy (Duchenne) and are building a robust portfolio of programs across muscle, central nervous system, and cardiac diseases. In 2023, we launched our fourth therapy and the first ever gene therapy to treat Duchenne. We’re looking for people who see unlimited potential in themselves and who are motivated by an unwavering commitment to patients.
What Sarepta Offers
At Sarepta, we care deeply about all the people in our community and believe in the importance of supporting them in all aspects of their lives. We aspire to maintain a culture that acknowledges people bring their whole selves to work, and we will strive to help everyone in our community integrate their work and personal lives while maintaining productivity. We are committed to offering a range of benefits and work-life resources designed to support people in the following areas:
- Physical and Emotional Wellness
- Financial Wellness
- Support for Caregivers
For a full list of our comprehensive benefits, see our website: https://www.sarepta.com/join-us
The Importance of the Role
The Associate Director of Biomarker Sciences assists in the oversight of clinical and non-clinical biomarker development across Sarepta’s pipeline. This role requires expertise in biomarker discovery, development, and implementation in clinical and non-clinical stage programs with emphasis on Sarepta’s siRNA pipeline. This role requires effective communication and collaboration, working with scientists and leaders across the company, partnering with external organizations and regulatory agencies. Working in a global matrix environment to support program needs and deliver on critical milestones, this role requires strong communication of scientific concepts including the relevance and design of various bio-assays and the data generated from them. The candidate will also support the preparation of regulatory submissions and data disseminations as needed. This role will also work cross-functionally to drive data analysis efforts and lead efforts to extract critical information from existing datasets.
Primary Responsibilities Include
- Assist the development and implementation of biomarker strategies consistent with the program development plans (nonclinical, translational and clinical) and regulatory strategies with emphasis on early and translational programs
- Collaborate with other functional leads (nonclinical, research operations, molecular biology) to support data generation efforts which support program biomarker strategies
- Conduct literature reviews to identify novel PK or PD biomarkers to support program needs and develop plan for implementation in non-clinical and clinical studies
- Perform extensive data analysis efforts to interpret non-clinical and clinical PD data and guide decision-making efforts
- Oversee Contract Research Organizations responsible for executing non-clinical and clinical data generation efforts including assay development and validation
- Represent Translational Biology on various internal functional sub-teams (clinical, non-clinical) and work cross-functionally to drive program milestones and participate in long-term planning efforts
- Aid in the generation of key materials for data disclosures (both internal and external) and participate in presentation efforts related to biomarker datasets and their interpretation
- Participate in regulatory writing efforts for translational and biomarker documents such as INDs, CTAs, and NDAs as well as assist with the completion of Requests for Information from regulatory agencies
More About You
Desired Education and Skills:
- PhD in Pharmacology, Biochemistry, Bioinformatics or related field with 4+ years of relevant experience in the biopharmaceutical industry focusing on translational research
- Expertise in neurobiology/neuromuscular biology, siRNA therapeutics, and drug development in the rare disease spaces
- Experience in development of bioassays, e.g., biomarkers with emphasis on protein-binding assay platforms
- Experience with big datasets and/or expertise in “-omics” platforms (RNASeq, Single cell, proteomics)
- Expertise in authoring and critically reviewing technical, clinical and regulatory documents
- Experience with qualification and validation of bioanalytical assays and biomarkers under FDA, EMA, ICH GCP/GLP and other applicable guidelines
- Experience in vendor management from quality, capability, data flow, interpretation, and reporting
- Demonstrated ability to work cross-functionally in a diverse matrixed environment
- Demonstrated ability to manage multiple complex projects simultaneously
- Exceptional verbal and written communication skills. Previous experience in outward facing roles is a plus.
What Now?
We’re always looking for solution-oriented, critical thinkers. So, if you’re comfortable with ambiguity and candor, relish challenging yourself, and place kindness and integrity at the forefront of how you approach your peers and work, then we encourage you to apply. This position is hybrid, you will be expected to work on site at one of Sarepta’s facilities in the United States and/or attend Company-sponsored in-person events from time to time.
The targeted salary range for this position is $152,800 - $191,000 per year. Sarepta is making a good faith effort to be transparent and accurate around our hiring ranges. The salary offer is commensurate with Sarepta’s compensation philosophy and considers factors including, but not limited to, education, training, experience, external market conditions, criticality of role, and internal equity. Candidates must be authorized to work in the U.S.
Sarepta Therapeutics offers a competitive compensation and benefit package.
Sarepta Therapeutics is an Equal Opportunity/Affirmative Action employer and participates in e-Verify.
Why Sarepta? Why Now?
The promise of genetic medicine has arrived, and Sarepta is at the forefront. We hold a leadership position in Duchenne muscular dystrophy (Duchenne) and are building a robust portfolio of programs across muscle, central nervous system, and cardiac diseases. In 2023, we launched our fourth therapy and the first ever gene therapy to treat Duchenne. We’re looking for people who see unlimited potential in themselves and who are motivated by an unwavering commitment to patients.
What Sarepta Offers
At Sarepta, we care deeply about all the people in our community and believe in the importance of supporting them in all aspects of their lives. We aspire to maintain a culture that acknowledges people bring their whole selves to work, and we will strive to help everyone in our community integrate their work and personal lives while maintaining productivity. We are committed to offering a range of benefits and work-life resources designed to support people in the following areas:
- Physical and Emotional Wellness
- Financial Wellness
- Support for Caregivers
For a full list of our comprehensive benefits, see our website: https://www.sarepta.com/join-us
The Importance of the Role
The Associate Director of Biomarker Sciences assists in the oversight of clinical and non-clinical biomarker development across Sarepta’s pipeline. This role requires expertise in biomarker discovery, development, and implementation in clinical and non-clinical stage programs with emphasis on Sarepta’s siRNA pipeline. This role requires effective communication and collaboration, working with scientists and leaders across the company, partnering with external organizations and regulatory agencies. Working in a global matrix environment to support program needs and deliver on critical milestones, this role requires strong communication of scientific concepts including the relevance and design of various bio-assays and the data generated from them. The candidate will also support the preparation of regulatory submissions and data disseminations as needed. This role will also work cross-functionally to drive data analysis efforts and lead efforts to extract critical information from existing datasets.
Primary Responsibilities Include
- Assist the development and implementation of biomarker strategies consistent with the program development plans (nonclinical, translational and clinical) and regulatory strategies with emphasis on early and translational programs
- Collaborate with other functional leads (nonclinical, research operations, molecular biology) to support data generation efforts which support program biomarker strategies
- Conduct literature reviews to identify novel PK or PD biomarkers to support program needs and develop plan for implementation in non-clinical and clinical studies
- Perform extensive data analysis efforts to interpret non-clinical and clinical PD data and guide decision-making efforts
- Oversee Contract Research Organizations responsible for executing non-clinical and clinical data generation efforts including assay development and validation
- Represent Translational Biology on various internal functional sub-teams (clinical, non-clinical) and work cross-functionally to drive program milestones and participate in long-term planning efforts
- Aid in the generation of key materials for data disclosures (both internal and external) and participate in presentation efforts related to biomarker datasets and their interpretation
- Participate in regulatory writing efforts for translational and biomarker documents such as INDs, CTAs, and NDAs as well as assist with the completion of Requests for Information from regulatory agencies
More About You
Desired Education and Skills:
- PhD in Pharmacology, Biochemistry, Bioinformatics or related field with 4+ years of relevant experience in the biopharmaceutical industry focusing on translational research
- Expertise in neurobiology/neuromuscular biology, siRNA therapeutics, and drug development in the rare disease spaces
- Experience in development of bioassays, e.g., biomarkers with emphasis on protein-binding assay platforms
- Experience with big datasets and/or expertise in “-omics” platforms (RNASeq, Single cell, proteomics)
- Expertise in authoring and critically reviewing technical, clinical and regulatory documents
- Experience with qualification and validation of bioanalytical assays and biomarkers under FDA, EMA, ICH GCP/GLP and other applicable guidelines
- Experience in vendor management from quality, capability, data flow, interpretation, and reporting
- Demonstrated ability to work cross-functionally in a diverse matrixed environment
- Demonstrated ability to manage multiple complex projects simultaneously
- Exceptional verbal and written communication skills. Previous experience in outward facing roles is a plus.
What Now?
We’re always looking for solution-oriented, critical thinkers. So, if you’re comfortable with ambiguity and candor, relish challenging yourself, and place kindness and integrity at the forefront of how you approach your peers and work, then we encourage you to apply. This position is hybrid, you will be expected to work on site at one of Sarepta’s facilities in the United States and/or attend Company-sponsored in-person events from time to time.
The targeted salary range for this position is $152,800 - $191,000 per year. Sarepta is making a good faith effort to be transparent and accurate around our hiring ranges. The salary offer is commensurate with Sarepta’s compensation philosophy and considers factors including, but not limited to, education, training, experience, external market conditions, criticality of role, and internal equity. Candidates must be authorized to work in the U.S.
Sarepta Therapeutics offers a competitive compensation and benefit package.
Sarepta Therapeutics is an Equal Opportunity/Affirmative Action employer and participates in e-Verify.
Job Roles at Sarepta Therapeutics
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Get Access To All JobsTips for Finding Sarepta Therapeutics Visa Sponsorship Jobs USA
Target roles that align with Sarepta's core research focus
Sarepta's pipeline centers on genetic medicine and rare neuromuscular diseases. Candidates with backgrounds in molecular biology, gene therapy, or RNA-targeted therapeutics are well-positioned for sponsored roles, align your application materials to these therapeutic areas specifically.
Understand which visa types Sarepta actively supports
Sarepta sponsors H-1B, Green Card (EB-2 and EB-3), F-1 OPT, and TN visas. Knowing which category fits your background before applying lets you frame your eligibility clearly in outreach and interviews with their talent acquisition team.
Start your search early if you're on OPT
Biotech hiring cycles in specialized therapeutic areas move on their own timelines. If you're on F-1 OPT with a hard cap-gap deadline, prioritize Sarepta early in your search so there's room to navigate H-1B cap filing without timeline pressure.
Focus on scientific, clinical, and regulatory functions
In biopharmaceutical companies like Sarepta, sponsored roles are concentrated in R&D, clinical operations, regulatory affairs, and CMC. Targeting these departments improves your odds compared to applying broadly across all business functions.
Use Migrate Mate to verify Sarepta's sponsorship history before applying
Sponsorship claims on job postings aren't always reliable. Migrate Mate surfaces verified sponsors with real filing history, so you can confirm Sarepta's track record and filter open roles by visa type before investing time in an application.
Be ready to discuss your work authorization status upfront
Biotech companies like Sarepta value efficiency in hiring. Being transparent about your visa type, current status, and any upcoming deadlines early in conversations helps their HR team assess sponsorship feasibility before the process goes far.
Frequently Asked Questions
Does Sarepta Therapeutics sponsor H-1B visas?
Yes, Sarepta Therapeutics sponsors H-1B visas and has a consistent track record of doing so across its scientific and corporate functions. Sponsored roles tend to concentrate in areas like research and development, clinical operations, and regulatory affairs, where specialized advanced-degree expertise is central to the work.
What visa types does Sarepta Therapeutics sponsor?
Sarepta Therapeutics sponsors H-1B visas, employment-based Green Cards (EB-2 and EB-3), F-1 OPT extensions, and TN visas for eligible Canadian and Mexican nationals. This range of visa types reflects a meaningful commitment to hiring international talent across multiple authorization pathways, particularly in technical and scientific roles.
Which departments or roles at Sarepta Therapeutics are most likely to be sponsored?
Sponsored roles at Sarepta are most commonly found in research and development, gene therapy and molecular science, clinical development, regulatory affairs, and CMC (chemistry, manufacturing, and controls). Corporate functions like finance, HR, and operations can also carry sponsorship, but the heaviest concentration is in scientific and clinical areas aligned with Sarepta's rare disease pipeline.
How do I find open sponsored jobs at Sarepta Therapeutics?
Migrate Mate is the most efficient way to find visa-sponsored jobs at Sarepta Therapeutics. It filters roles by verified sponsorship history, so you're not guessing whether a posting actually supports work visa candidates. Browse Sarepta's profile on Migrate Mate to see current openings filtered by the visa types they actively sponsor.
How do I approach the application process at Sarepta Therapeutics as a visa-sponsored candidate?
Apply to roles closely matched to Sarepta's core focus areas, particularly genetic medicine and rare neuromuscular disease research, where your technical expertise carries the most weight. Be upfront about your visa status and timeline early in the recruitment process. Sarepta works with immigration counsel on sponsorship logistics, so clarity on your situation helps both sides move efficiently.