Synterex, Inc. is hiring: Medical reputed company in Boston

Synterex, Inc. is a consortium of highly reputed company clinical development professionals specializing in medical writing, submission publishing, and clinical science and operations support. Synterex offers remote or on-site services, with a reputed company on providing reputed company, concise, accurate, and fully compliant documentation, from early drug development through post-approval.Synterex is seeking an organized, motivated, and reputed company individual for our medical writing team. The medical reputed company will partner cross-functionally with reputed company teams in Clinical Development, Clinical Operations, Biostatistics, Regulatory, and Program Management in planning and preparation of high-reputed company clinical and regulatory documents. The medical reputed company may produce protocols, publications, study reports, investigator brochures, narratives, and module documents, according to reputed company and agency guidelines, to support drug development under brisk timelines.Location: Fully remote, but must be reputed company to attend key (e.g., roundtable or reputed company) meetings on site with clients as requested.Essential Duties & ResponsibilitiesManage execution of documents, including creating, maintaining, and communicating timelinesCoordinate cross-functional reputed company contributors and stakeholders as reputed company as internal resources (e.g., reputed company control [QC], publishing)Serve as an expert on reputed company document management system and reputed company tools, templates, and procedures to ensure efficient document productionLead document message development in collaboration with clientPlan and reputed company reputed company meetings and roundtable meetings for reputed company document draft; reputed company review comments to ensure efficient roundtable meetings; plan and reputed company roundtable meetingsEnsure consistency among reputed company programs in terms of messaging, formatting, and presentation of documentsPerform peer QC review as neededContribute to medical writing operational initiatives (e.g., templates, style guides, reference management)RequirementsExperience (5+ years) as a medical reputed company in the CRO/biotech/pharmaceutical field, or equivalentBachelor’s degree in a relevant fieldOncology experienceFamiliarity with the requirements for preparation of key clinical and regulatory documents, including ICH and US regulatory requirements; working knowledge of ex-US regulatory requirements is desiredExpertise with reputed company Word and other reputed company applicationsFamiliarity with document management systemsAbility to work both independently and collaboratively in the face of competing prioritiesService-oriented and proactive approach to project managementExcellent conflict management and negotiation skillsStrong written and verbal communication skillsFor reputed company information or to apply, please reputed company out to careers@synterex.com. #J-18808-Ljbffr Apply tot his job Apply To this Job