Sr. Manager, Scientific Writing

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    "requisitionDescription": "<div><div><p data-pasted=\"true\"><span style=\"font-family: arial, sans-serif; font-size: 14px; color: rgb(0, 0, 0);\">Reporting to the Director, Scientific Communications, the Sr. Manager, Scientific Writing is responsible for developing high-quality scientific resources (e.g., abstracts, posters, publications) that clearly and concisely communicate scientific data on Kiniksa&rsquo;s products and therapeutic areas of interest. Further, h/she will ensure all deliverables remain aligned with Kiniksa strategy and tactics. The Sr. Manager, Scientific Writing works closely with Medical Affairs colleagues to inform and execute medical strategies aligned with program and corporate priorities. This position will work regularly with the internal cross-functional team on material to be used in writing scientific articles, abstracts, and posters.</span></p><p><span style=\"font-family: arial, sans-serif; font-size: 14px; color: rgb(0, 0, 0);\"><strong>Responsibilities (including, but not limited to):</strong></span></p><p><span style=\"font-family: arial, sans-serif; font-size: 14px; color: rgb(0, 0, 0);\">&bull; In close collaboration with the Medical Director and RWE, support concept development and framing of scientific communication deliverables (e.g., abstracts, posters, publications)</span></p><p><span style=\"font-family: arial, sans-serif; font-size: 14px; color: rgb(0, 0, 0);\">&bull; Lead scientific writing and editing of scientific communication deliverables</span></p><p><span style=\"font-family: arial, sans-serif; font-size: 14px; color: rgb(0, 0, 0);\">&bull; Remain up-to-date on overall strategy for Kiniksa&rsquo;s assets and ensure all deliverables remain aligned with strategic aims</span></p><p><span style=\"font-family: arial, sans-serif; font-size: 14px; color: rgb(0, 0, 0);\">&bull; Lead operational oversight for all scientific communication projects, including timely dissemination of materials for both internal and external author reviews, and strict adherence to deadlines for deliverable submissions</span></p><p><span style=\"font-family: arial, sans-serif; font-size: 14px; color: rgb(0, 0, 0);\">&bull; Contribute to the planning and execution of medical and scientific information for Kiniksa products within multiple therapeutic areas</span></p><p><span style=\"font-family: arial, sans-serif; font-size: 14px; color: rgb(0, 0, 0);\">&bull; Support the execution of the strategic publication plans for each program</span></p><p><span style=\"font-family: arial, sans-serif; font-size: 14px; color: rgb(0, 0, 0);\">&bull; In collaboration with internal stakeholders, assist in the management of publication plans across the portfolio, ensuring consistency and medical accuracy as well as compliance with current good publication practice guidelines</span></p><p><span style=\"font-family: arial, sans-serif; font-size: 14px; color: rgb(0, 0, 0);\">&bull; Ensure content is scientifically and clinically sound and well-organized while maintaining consistency in terminology, tone, and document structure as it relates to Kiniksa&rsquo;s ideology</span></p><p><span style=\"font-family: arial, sans-serif; font-size: 14px; color: rgb(0, 0, 0);\">&bull; Provide oversight for document quality checks, managing timelines, data analysis and interpretation, and preparation of publication-quality figures</span></p><p><span style=\"font-family: arial, sans-serif; font-size: 14px; color: rgb(0, 0, 0);\">&bull; Proactively seek input from Medical Affairs team members (including Chief Medical Officer), and cross-functional colleagues to plan the content for internal documents or publications</span></p><p><span style=\"font-family: arial, sans-serif; font-size: 14px; color: rgb(0, 0, 0);\">&bull; Review and amend work in response to internal and external feedback</span></p><p><span style=\"font-family: arial, sans-serif; font-size: 14px; color: rgb(0, 0, 0);\">&bull; Lead company-wide literature surveillance and remain up-to-date on all relevant emerging literature</span></p><p><span style=\"font-family: arial, sans-serif; font-size: 14px; color: rgb(0, 0, 0);\">&bull; Support the development and maintenance of Scientific Communications Platform(s)</span></p><p><span style=\"font-family: arial, sans-serif; font-size: 14px; color: rgb(0, 0, 0);\">&bull; Proof, format, and edit internal documents as appropriate</span></p><p><span style=\"font-family: arial, sans-serif; font-size: 14px; color: rgb(0, 0, 0);\">&bull; Assist in ensuring that policies and procedures applicable to scientific communications are kept current and align with good publication practices</span></p><p><span style=\"font-family: arial, sans-serif; font-size: 14px; color: rgb(0, 0, 0);\"><strong>Qualifications</strong></span></p><p><span style=\"font-family: arial, sans-serif; font-size: 14px; color: rgb(0, 0, 0);\">&bull; Advanced scientific degree (PhD, PharmD, MD) strongly preferred or relevant advanced science degree (MS, MPH, or other scientific or clinical degrees also considered)</span></p><p><span style=\"font-family: arial, sans-serif; font-size: 14px; color: rgb(0, 0, 0);\">&bull; A minimum of 2+ years of document writing and publication experience in the bio/pharmaceutical industry or related experience (e.g., scientific/medical communications agency) is required</span></p><p><span style=\"font-family: arial, sans-serif; font-size: 14px; color: rgb(0, 0, 0);\">&bull; Strong scientific writing skills including editing experience, data quality review, and a proven track record of taking publications from conception to publication (autoimmune experience is a plus)</span></p><p><span style=\"font-family: arial, sans-serif; font-size: 14px; color: rgb(0, 0, 0);\">&bull; Ability to explain complex scientific and clinical concepts clearly for various audiences</span></p><p><span style=\"font-family: arial, sans-serif; font-size: 14px; color: rgb(0, 0, 0);\">&bull; Working knowledge of statistics, data analysis and data interpretation</span></p><p><span style=\"font-family: arial, sans-serif; font-size: 14px; color: rgb(0, 0, 0);\">&bull; Experience creating publication quality figures</span></p><p><span style=\"font-family: arial, sans-serif; font-size: 14px; color: rgb(0, 0, 0);\">&bull; Experience working with publication management software (PubsHub)</span></p><p><span style=\"font-family: arial, sans-serif; font-size: 14px; color: rgb(0, 0, 0);\">&bull; Strong understanding of the drug development process</span></p><p><span style=\"font-family: arial, sans-serif; font-size: 14px; color: rgb(0, 0, 0);\">&bull; Strong understanding of current good publication practices and ICMJE criteria (CMPP certification is a plus)</span></p><p><span style=\"font-family: arial, sans-serif; font-size: 14px; color: rgb(0, 0, 0);\">&bull; Ability to demonstrate a solid understanding of process for submission of abstracts and manuscripts to scientific congresses and journals, respectively</span></p><p><span style=\"font-family: arial, sans-serif; font-size: 14px; color: rgb(0, 0, 0);\">&bull; Ability to collaborate effectively with internal stakeholders and external authors</span></p><p><span style=\"font-family: arial, sans-serif; font-size: 14px; color: rgb(0, 0, 0);\">&bull; Excellent verbal and written communication skills</span></p><p><span style=\"font-family: arial, sans-serif; font-size: 14px; color: rgb(0, 0, 0);\">&bull; Ability to work under deadlines in a fast-paced environment with a high degree of flexibility</span></p><p><span style=\"font-family: arial, sans-serif; font-size: 14px; color: rgb(0, 0, 0);\">&bull; Ability to effectively facilitate meetings and manage cross-functional teams</span></p><p><span style=\"font-family: arial, sans-serif; font-size: 14px; color: rgb(0, 0, 0);\">&bull; Ability to work with minimal supervision and function effectively as a team member; a self-starter</span></p><p><span style=\"font-family: arial, sans-serif; font-size: 14px; color: rgb(0, 0, 0);\">&bull; Project management experience (timelines, planning, workflows, creation of reports, archiving)</span></p><p><span style=\"font-family: arial, sans-serif; font-size: 14px; color: rgb(0, 0, 0);\">&bull; Must exhibit characteristics that exemplify drive, passion and focus that will translate into significant contributions towards building a global generational company</span></p><p><span style=\"font-family: arial, sans-serif; font-size: 14px; color: rgb(0, 0, 0);\">&bull; Must show the ability to multi-task and change course quickly</span></p><p><span style=\"font-family: arial, sans-serif; font-size: 14px; color: rgb(0, 0, 0);\">&bull; Proficiency with Microsoft Office applications including Microsoft CoPilot</span></p><p><span style=\"font-size: 14px; color: rgb(0, 0, 0); font-family: arial, sans-serif;\" data-pasted=\"true\">The pay range for this position is $192,000 - $201,000. Compensation is subject to change commensurate with industry standards and the candidate&rsquo;s relevant experience and qualifications.&nbsp;</span></p><p><span data-pasted=\"true\"><span style=\"margin: 0px; padding: 0px; color: rgb(0, 0, 0); font-style: normal; font-weight: 400; text-indent: 0px; text-transform: none; font-size: 14px; line-height: 19px; font-family: arial, sans-serif;\" data-pasted=\"true\"><span style=\"margin: 0px; padding: 0px;\">Kiniksa is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, transgender status, age, genetics, national origin, protected veteran status, or disability status, or any other legally protected category. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.</span></span></span></p></div></div>\n",
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