Flexible Spending Accounts for medical expenses and dependent care expenses.Highly competitive and inclusive medical, dental and vision coverage options.Moderna is pleased to provide you and your family with a comprehensive and innovative suite of benefits, including: Hybrid work arrangement available for those local to our Cambridge, MA headquarters or fully remote within the US with ability to travel onsite as necessary Will work collaboratively with multifunctional teams and partners and will be relentless in pursuing successful outcomes Strong organizational/prioritization skills for the management of multiple concurrent projectsĭemonstrated proficiency with word processing, spreadsheet, database, presentation software (MS Office skills such as Outlook, Word, Excel, PowerPoint, and SharePoint) and experience and skill performing medical literature searches Strong project management and organizational skills Minimum of six years medical writing experience with a total of more than 10 years of pharmaceutical or biotech experience requiredĮxcellent written communication skills and attention to detail related to consistency, grammar, syntax, and accuracyĮxperience producing high quality clinical and regulatory submission documents Minimum of bachelor's degree or equivalent in scientific or medical discipline Advanced degree preferred Provide support for QC of complex clinical documents Lead significant workstreams that involve work across departments or with external vendors Manage timelines and communicate with team stake holders to maintain awareness of expectations, milestones, and deliverables. Plan and coordinate timelines to ensure timely completion of clinical writing projects.
Serve as the medical writing Lead contributing to a variety of clinical documents for clinical and regulatory purposes, including clinical protocols, clinical study reports, investigator brochures, and other regulatory submissions documents.Ĭoordinate the efforts of cross-functional teams to produce high-quality, scientifically accurate documents. The successful candidate will be detailed oriented, self-directed and with the ability to be flexible and manage workload to meet project timelines. The Clinical Development team at Moderna is looking for an agile, self-motivated, and experienced Associate Director to serve as an integral part of the Medical Writing Team to support clinical project teams to meet their clinical document deliverables. Associate Director, Medical Writing (Hybrid or Remote) page is loaded Associate Director, Medical Writing (Hybrid or Remote) Apply locations Cambridge, Massachusetts Clinical Development time type Full time posted on Posted 4 Days Ago job requisition id R11025
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