Why Sarepta? Why Now?
The promise of genetic medicine has arrived, and Sarepta is at the forefront. We hold leadership positions in Duchenne muscular dystrophy (DMD) and limb-girdle muscular dystrophies (LGMDs), and we currently have more than 40 programs in various stages of development in gene therapy, RNA and gene editing. 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

Nonclinical strategy and report management (NSRM) is a cross-functional group supporting nonclinical regulatory submissions and preparation of nonclinical documents. NSRM works with nonclinical research, nonclinical safety, immunology, regulatory, QC/QA and research operations groups to produce scientifically accurate and compliant documents including but not limited to SOPs, manuscripts, protocols, study reports, investigator brochures, IND and BLA modules.
The nonclinical strategy and report management Scientist will primarily support the progression of a nonclinical program from research phase to development. This involves aiding in the compilation of nonclinical reports for an Investigational New Drug (IND) application. The nonclinical strategy and report management Scientist will be responsible for nonclinical data quality in reports submitted for regulatory filings, literature searches and reference checks, and drafting of study reports. The scientist will also be responsible for assisting in data interpretation and figure generation for reporting and may assist in statistical analysis of final data sets. Additional responsibilities include storyboard preparation and risk mitigation through collaborative problem solving. The position may shadow and potentially assist with in-lab activities on a limited basis to effectively perform their role. In collaboration with reporting leads, the nonclinical strategy and report management Scientist will be responsible for the management of study reports that will be used for internal purposes as well as for regulatory submissions.

The Opportunity to Make a Difference

Aids in preparation of complex nonclinical and regulatory documents to support IND submissions including, but not limited to, protocols, study reports, amendments, investigator brochures, eCTD formatting, eCTD table and figure formatting, and IND/IMPD sections.Reviews experimental results and interpretation of nonclinical dataScientific contributor and subject matter expert who interprets data and applies knowledge of regulatory and scientific requirements to support document preparationEffectively collaborates with cross-functional teams to produce clearly written, high-quality, and scientifically accurate documents and ensure consistency between related documentsHigh competency in writing, editing, and reviewing nonclinical and regulatory documents per company and other guidelinesEnsures accuracy of data reported in documents being filed with regulatory agenciesPerforms and/or assists with quality control peer reviews of nonclinical documentsIdentifies opportunities to improve operational efficiency and compliance and assesses regulatory guidelines for impact to nonclinical studies.Demonstrated   critical   thinking and creative problem-solving skills across a range of scientific disciplines,  including  a  constant  grounding  in  analyses

More about You

PhD with experience in cellular or molecular biology or related disciplineExcellent writing, presentation, and project management skillsMeticulous attention to detail and ability to comply with company style guides and templatesAbility to create strong, collaborative working relationships, operating as part of a teamProficient in Graphpad Prism, RStudio/Python, Microsoft Excel, and Microsoft WordCompetent applying common statistical tests for data analysisExcited to implement knowledge of FDA/international regulations, ICH guidelines, and applicable regulatory processes related to document preparation and production

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.
 

#LI-Onsite

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This position requires work on site at one of Sarepta’s facilities in the United States.

The targeted salary range for this position is $102,800 - $128,500 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.