Medical Writing Science Senior Manager (Hybrid)

Skip to main contentSign InMedical Writing Science Senior Manager (Hybrid) page is loadedMedical Writing Science Senior Manager (Hybrid)ApplylocationsBoston, MAtime typeFull timeposted onPosted 30+ Days Agojob requisition idREQ-27670Job DescriptionGeneral Summary:The Medical Writing Science Senior Manager is responsible for independently authoring complex clinical study documents and sections of regulatory submissions to support all phases of clinical drug development. This role may represent Medical Writing Science as a cross-functional team member for study-level and program-level activities.This is a hybrid role which allows for 2 days per week remote work and 3 days per week in the Boston Fan Pier office.Key Duties and Responsibilities:Authors complex clinical regulatory documents (e.g., clinical study protocols, clinical study reports, investigator’s brochures, documents to support meetings with regulatory agencies, and sections of marketing authorization applications) in partnership with key stakeholdersServes as the lead Medical Writing Scientist for complex or pivotal clinical studies for multiple programs or therapeutic areasProvides expert review of study-level and program-level documentsParticipates in developing key messages for complex clinical regulatory documentsProvides leadership on teams responsible for defining the direction and regulatory strategy for a clinical development programProvides strategic and scientific contributions to regulatory documentation in support of the clinical development pipelineContributes to content and strategy of presentations for regulatory agency advisory committee meetings; may prepare advisory committee briefing documentsEnsures document preparation is compliant with company and industry standardsStrong contributor on cross-functional teams working on standard operating procedures, process improvements, and integration of new tools and technologiesKnowledge and Skills:Outstanding written and oral communication skillsExtensive experience writing and editing clinical regulatory documentsAbility to analyze, interpret, and summarize highly complex dataAdvanced understanding of drug development, clinical research, study designs, biostatistics, pharmacology, regulatory requirements, and medical terminologyAbility to mediate conflicts by negotiating, compromising, persuading, and facilitating the open exchange of ideas and opinionsHighly developed project management and organizational skillsAbility to manage challenging, high-value projectsInitiative and creativity in solving complex problems; ability to have a substantial role in developing and implementing improvements in cross-functional processesEducation and Experience:Bachelor's degree in relevant disciplinePh.D. (or equivalent degree)Typically requires 6 years of experience or the equivalent combination of education and experience.#LI-AR1#LI-HybridPay Range:$137,200 - $205,800Disclosure Statement:The range provided is based on what we believe is a reasonable estimate for the base salary pay range for this job at the time of posting. This role is eligible for an annual bonus and annual equity awards. Some roles may also be eligible for overtime pay, in accordance with federal and state requirements. Actual base salary pay will be based on a number of factors, including skills, competencies, experience, and other job-related factors permitted by law.At Vertex, our Total Rewards offerings also include inclusive market-leading benefits to meet our employees wherever they are in their career, financial, family and wellbeing journey while providing flexibility and resources to support their growth and aspirations.  From medical, dental and vision benefits to generous paid time off (including a week-long company shutdown in the Summer and the Winter), educational assistance programs including student loan repayment, a generous commuting subsidy, matching charitable donations, 401(k) and so much more.Flex Designation:Hybrid-Eligible...