The qualified candidate will provide laboratory support of day-to-day GCLP / GLP testing on . This book will support your growth as a biotechnology professional. In-House Counsel jobs. The compay's goal is to harness the power of cutting-edge technology to improve the lives of people affected by rare, infectious and other diseases. Non-GAAP research and development expenses are defined by the Company as GAAP research and development expenses excluding depreciation and amortization expense, stock-based compensation expense and other items. The Duchenne Account 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 indication is approved under accelerated approval based on an increase in dystrophin production in skeletal muscle observed in patients treated with AMONDYS 45. Send me new remote jobs everyday: All Jobs Sarepta Therapeutics Jobs . The Company: Sarepta Therapeutics, Inc. (NASDAQ: SRPT) is at the forefront of precision genetic medicine, having built a world leading pipeline for the treatment of Duchenne muscular dystrophy (DMD. Careers Careers. 2018 number of employees: 499. Kidney function should be monitored in patients taking VYONDYS 53. In February 2021, the Company entered into an agreement to sell the rare pediatric disease Priority Review Voucher (PRV) it received from the FDA in connection with the approval of AMONDYS 45. $18.7 million increase in the offset to expense associated with a collaboration reimbursement from Roche primarily due to continuing development of the Company’s SRP-9001 micro-dystrophin gene therapy. Are Sarepta Therapeutics employees satisfied with their compensation? Sarepta Therapeutics. Get hired! The decrease in research and development expenses primarily reflects the following: Research and development expenses were $573.9 million for the nine months ended September 30, 2021, compared to $515.1 million for the same period of 2020, an increase of $58.8 million. Sarepta Therapeutics, Inc., the leader in precision genetic medicine for rare diseases, announced that it has priced an underwritten public offering of 6,172,840 shares of its common stock at a price to the public of $81.00 per share. Sarepta's Genetic Therapies Center of Excellence - Building Exterior The new, state-of-the-art research facility encompasses 85,000 square feet and significantly expands Sarepta's global . For more information, please visit www.sarepta.com or follow us on Twitter, LinkedIn, Instagram and Facebook. For the nine months ended September 30, 2021 and 2020, other expense, net was $52.4 million and $34.2 million, respectively. Don't miss what's happening in your neighborhood. This timely, comprehensive volume draws on recent advances in molecular, cellular and organismal biology to provide a detailed analysis of the phylogeny and ontogeny of the immune system. $9.3 million decrease in professional service expenses primarily due to a decrease in reliance on third-party selling, general and administrative contractors; $4.8 million decrease in compensation and other personnel expenses primarily due to a net decrease in headcount period over period; $1.6 million decrease in stock-based compensation expense primarily due to changes in headcount and stock prices; and. Who We Are Sarepta is a global biotechnology company on an urgent mission: to. Report this job. Full-time, Part-time. Sarepta Therapeutics annual revenue for . Sarepta Therapeutics, headquartered in Cambridge, Massachusetts, is a commercial-stage biopharmaceutical company focused on the discovery and development of unique RNA-targeted therapeutics for the treatment of rare neuromuscular diseases. The decrease is primarily driven by cash used to fund the Company’s ongoing operations during 2021. This book provides the answers to enable all aspects of the people function to perform to their full potential. Redefining HR is a refreshing take on the evolution of the field of Human Resources and People Operations. Sarepta Therapeutics. tsorrentino@sarepta.com, © 1985 - 2021 BioSpace.com. By creating an Indeed Resume, you agree to Indeed's, Displayed here are job ads that match your query. Apply to Quality Assurance Analyst, Operations Manager, Clinical Associate and more! Set up and maintain manual and computerized information filing systems. The Company evaluates other items of expense and income on an individual basis. The Company uses these non-GAAP measures as key performance measures for the purpose of evaluating operational performance and cash requirements internally. Senior Sales Recruiter jobs. The increase in research and development expenses primarily reflects the following: Non-GAAP research and development expenses were $115.1 million and $159.9 million for the three months ended September 30, 2021 and 2020, respectively, a decrease of $44.8 million. Cost of sales (excluding amortization of in-licensed rights) (unaudited, in thousands, except share and per share data), Investor Contact: [Operator instructions] As a reminder, today's program is being recorded. Sarepta Therapeutics Andover, MA 2 weeks ago Be among the first 25 applicants See who Sarepta Therapeutics has hired for this role Manager, Talent Acquisition 2021-10-23. The qualified candidate will provide laboratory support of day-to-day GCLP/GLP testing on muscle/nerve and other tissue types using complex histology methods in accordance with the requirements of approved protocols; maintains records of experiments; assists in analyzing data and prepares . All content is posted anonymously by employees working at Sarepta Therapeutics. as part of its Gene Therapy Center of Excellence. This book is a valuable reference for professionals in microbiology, epidemiology, public health, and clinical and veterinary medicine. Known risk factors include the following: we may not be able to comply with all FDA post-approval commitments and requirements with respect to our products in a timely manner or at all; success in preclinical and clinical trials, especially if based on a small patient sample, does not ensure that later clinical trials will be successful, and the results of future research may not be consistent with past positive results or may fail to meet regulatory approval requirements for the safety and efficacy of product candidates; certain programs may never advance in the clinic or may be discontinued for a number of reasons, including regulators imposing a clinical hold and us suspending or terminating clinical research or trials; if the actual number of patients suffering from the diseases we aim to treat is smaller than estimated, our revenue and ability to achieve profitability may be adversely affected; we may not be able to execute on our business plans, including meeting our expected or planned regulatory milestones and timelines, research and clinical development plans, and bringing our product candidates to market, for various reasons, some of which may be outside of our control, including possible limitations of company financial and other resources, manufacturing limitations that may not be anticipated or resolved for in a timely manner, the COVID-19 pandemic and regulatory, court or agency decisions, such as decisions by the United States Patent and Trademark Office with respect to patents that cover our product candidates; and those risks identified under the heading “Risk Factors” in our most recent Annual Report on Form 10-K for the year ended December 31, 2020 and most recent Quarterly Report on Form 10-Q filed with the Securities and Exchange Commission (SEC) as well as other SEC filings made by the Company which you are encouraged to review.
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