Sarepta Therapeutics
Senior Manager, Global Scientific Communications
Sarepta Therapeutics, Cambridge, Massachusetts, us, 02140
Senior Manager, Global Scientific Communications
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 OffersAt 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 WellnessFinancial WellnessSupport for CaregiversFor a full list of our comprehensive benefits, see our website:
https://www.sarepta.com/join-usThe Importance of the RoleThe Sr. Manager, Global Scientific Communications is responsible for the development of high-quality scientific publications (i.e. clinical, scientific, and health economics manuscripts, abstracts, posters, and oral presentations) in accordance with authors’ direction and in adherence to Sarepta’s Publication Standard Operating Procedure and industry guidelines. The Sr. Manager may contribute to the creation of other scientific communication documents and projects, as assigned.The Opportunity to Make a DifferenceServe as lead on scientific publications (abstracts, posters, presentations, and manuscripts) and work with authors, evidence generation teams, and medical communication agencies on the timely execution of publication plans, ensuring a high-quality and timely product, as well as adherence to publication SOP and associated procedures.Support development and revision of publication plans for assigned products in line with brand strategies and priorities.Review draft publications for scientific quality, data accuracy, and ensure alignment with author direction.Support cross-functional alignment across relevant internal stakeholders and ensure coordination of the review, approval, and other applicable activities related to the development of scientific publication projects.Interface with external experts (e.g., physicians, other health care professionals, health economists) and effectively collaborate with cross-functional teams.Communicate publication development process, industry guidance on good publication practices, and authorship criteria to team members as needed.Support/lead the development/maintenance of assigned scientific communication platforms.Contribute to the creation of slide-decks, content development, and related activities.Understand, assimilate, and interpret sources of information with appropriate guidance from authors and product team members; interpret and explain data generated from a variety of sources, including internal and external studies, research documentation, charts, graphs, and tables, and verify that results are consistent with study data; convert relevant data and information into a form that meets publication needs, ensuring required documentation is obtained in adherence to Publication Procedures, ICMJE, and GPP3 guidelines.Perform other related duties as needed.More about YouAdvanced Scientific Degree (Ph.D., PharmD) required. Master’s Degree will be considered with significant publication planning and writing experience. Relevant professional certification/credential (e.g., CMPP, AMWA) is a plus.At least 5 years of medical/scientific publication planning and development experience in the pharmaceutical/biotech industry or medical communication agencies.Ability to understand and interpret scientific data.Excellent organizational, interpersonal, and communications (verbal, written, presentation) skills with flawless attention to detail.Good understanding of industry guidelines associated with scientific publications.Working knowledge of statistical concepts.Proficient with Microsoft Windows, Word, Excel, and PowerPoint.Experience in working with fast-paced, collaborative, cross-functional teams.Ability to travel to up to 20%.Experience in rare disease/neurology therapeutic area.Experience with publication tracking software (iEnvision).Experience in developing HEOR, real-world evidence, or patient-reported outcomes publications.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 remote. However, 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 $132,000 - $165,000 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.
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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 OffersAt 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 WellnessFinancial WellnessSupport for CaregiversFor a full list of our comprehensive benefits, see our website:
https://www.sarepta.com/join-usThe Importance of the RoleThe Sr. Manager, Global Scientific Communications is responsible for the development of high-quality scientific publications (i.e. clinical, scientific, and health economics manuscripts, abstracts, posters, and oral presentations) in accordance with authors’ direction and in adherence to Sarepta’s Publication Standard Operating Procedure and industry guidelines. The Sr. Manager may contribute to the creation of other scientific communication documents and projects, as assigned.The Opportunity to Make a DifferenceServe as lead on scientific publications (abstracts, posters, presentations, and manuscripts) and work with authors, evidence generation teams, and medical communication agencies on the timely execution of publication plans, ensuring a high-quality and timely product, as well as adherence to publication SOP and associated procedures.Support development and revision of publication plans for assigned products in line with brand strategies and priorities.Review draft publications for scientific quality, data accuracy, and ensure alignment with author direction.Support cross-functional alignment across relevant internal stakeholders and ensure coordination of the review, approval, and other applicable activities related to the development of scientific publication projects.Interface with external experts (e.g., physicians, other health care professionals, health economists) and effectively collaborate with cross-functional teams.Communicate publication development process, industry guidance on good publication practices, and authorship criteria to team members as needed.Support/lead the development/maintenance of assigned scientific communication platforms.Contribute to the creation of slide-decks, content development, and related activities.Understand, assimilate, and interpret sources of information with appropriate guidance from authors and product team members; interpret and explain data generated from a variety of sources, including internal and external studies, research documentation, charts, graphs, and tables, and verify that results are consistent with study data; convert relevant data and information into a form that meets publication needs, ensuring required documentation is obtained in adherence to Publication Procedures, ICMJE, and GPP3 guidelines.Perform other related duties as needed.More about YouAdvanced Scientific Degree (Ph.D., PharmD) required. Master’s Degree will be considered with significant publication planning and writing experience. Relevant professional certification/credential (e.g., CMPP, AMWA) is a plus.At least 5 years of medical/scientific publication planning and development experience in the pharmaceutical/biotech industry or medical communication agencies.Ability to understand and interpret scientific data.Excellent organizational, interpersonal, and communications (verbal, written, presentation) skills with flawless attention to detail.Good understanding of industry guidelines associated with scientific publications.Working knowledge of statistical concepts.Proficient with Microsoft Windows, Word, Excel, and PowerPoint.Experience in working with fast-paced, collaborative, cross-functional teams.Ability to travel to up to 20%.Experience in rare disease/neurology therapeutic area.Experience with publication tracking software (iEnvision).Experience in developing HEOR, real-world evidence, or patient-reported outcomes publications.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 remote. However, 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 $132,000 - $165,000 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.
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