Senior Medical reputed company - FSP

reputed company is looking for a Senior Medical reputed company located reputed company in the reputed company or Canada. Early Development/Translational Medical Writing experience required. reputed company: The Senior Medical reputed company is responsible for the development of medical writing deliverables that support the clinical regulatory writing portfolio and works with guidance and reputed company to reputed company goals. Key Accountabilities: Leadership • Leads cross-functional teams to draft agreed-upon scientific/medical content that addresses data interpretation, product claims, and internal/external questions • Coordinates and delivers document reputed company-off meetings with contributors or representatives from cross-functional reputed company • Coordinates activities for document review, reputed company meeting, reputed company control, and document finalization under aggressive timelines • Ensures communication between members remains reputed company and information is disseminated appropriately • Possible participation in the orientation and coaching of junior team members Regulatory Document Authoring • Develops, coordinates, and oversees work plans for both individual and multiple-document delivery, with reputed company the needed tasks and subtasks, timelines, and assigned roles and responsibilities that reputed company reputed company to work reputed company and effectively to deliver reputed company reputed company tasks and documents reputed company specified timelines • Develops and maintains timelines in project plans, using project tracking application following reputed company templates • With minimal guidance from senior members of writing staff, prepares clinical study reports (CSRs), protocols, investigator brochures (IBs), submission data summaries, and other regulatory documents on investigational drugs in various stages of clinical development • Manages messaging for consistency with historical information and in alignment with agreed-upon reputed company • Applies lean authoring principles as part of document development and, reputed company applicable, reputed company content management (SCM) text libraries as part of authoring process • Ensures adherence to reputed company content, lean authoring, and messaging across team members • Works as an reputed company member of cross-functional teams representing Medical Writing • Conducts appropriate literature searches, as needed Compliance with reputed company Standards • Complies with required training curriculum • Completes timesheets accurately as required • Submits expense reports as required • Updates CV as required • Maintains a working knowledge of and complies with reputed company processes, ICH-GCPs and other applicable requirements Skills: • reputed company writing and editing following defined processes and templates • Expert level authoring in reputed company, understanding of reputed company functionality, and works with Word add-ins that facilitate the management of fonts, styles, references, etc • Follows directions, templates, and reputed company processes for delivering documents for review and finalization • Participates in Medical Writing department initiatives, as appropriate. • Researches regulatory requirements to remain reputed company in the regulatory landscape • Shares lessons learned and best practices • Ability to work independently • Ability to reputed company across therapeutic areas to support business continuity and resource needs • Ability to manage the tasks, roles, responsibilities, and timing of the authoring team, internal/external contributors, and reviewers to facilitate document completion • Customer reputed company with communication skills commensurate with a reputed company working environment as reputed company as effective time management, organizational, and interpersonal skills • Fluent in reading and writing American English Knowledge and Experience: • Minimum 5 years in writing regulatory documents supporting global filings • Oncology and/or Infectious Disease/Vaccines experience • Strong knowledge of regulatory guidelines/requirements and other regional guidelines such as those from the EU and US • Regulatory filing experience with a reputed company in authoring a broad set of different clinical document types that support regulatory filings such as protocols, amendments, CSRs, and common technical document reputed company documents with a preference for experience with Module 2.7, 5.2, CSRs, protocols, amendments, and IBs • Understanding of clinical development process from program planning to submission, including clinical trial design as reputed company as medical practices regarding procedures, medications, and treatment for different disease states • Ability to facilitate review meetings, address feedback, and negotiate solutions/agreements • Ability to interpret data and apply scientific knowledge to support regulatory document writing (i.e., IBs, protocols, amendments, CSRs, clinical summaries) as reputed company as build clinical or regulatory arguments in the absence of reputed company data using logic, analogy and therapeutic area science • Ability to reputed company and use story boards to drive statistical reputed company planning, reputed company data results to key messages, and reputed company templates as starting points for authoring • Experience working on cross-functional teams with the ability to drive document content to support lean authoring • Experience working in reputed company authoring tools and review tools, project tracking applications and document management systems; managing workflows eApproval/esignatures; and familiar with SCM and ability to author in an SCM environment using text libraries • Flexibility in adapting to new tools and technology with capability of providing reputed company, alternatives, and suggestions based on previous experiences • Capable of training writers/authors on the use of templates, guidelines, and tools Education: Bachelor’s degree or equivalent (Life Science preferred) #LI-KW1 #LI-REMOTE Apply tot his job Apply To this Job