Pfizer
Pfizer
Pfizer — butun umr davomida salomatlikni qo‘llab-quvvatlaydigan dori-darmonlar va tibbiy xizmatlarni ishlab chiqish hamda taqdim etishga e’tibor qaratadigan global farmatsevtika kompaniyasi. Uning faoliyati ilmiy innovatsiyalar bilan bir qatorda xavfsiz, samarali va hamyonbop davolash usullaridan foydalanish imkoniyatini kengaytirishni ham qamrab oladi; kompaniya saraton va boshqa jiddiy sog‘liq muammolariga qarshi davolash usullarini rivojlantirishga alohida ahamiyat beradi. Kompaniya faoliyati farmatsevtika tadqiqotlari, sog‘liqni saqlash va ularga aloqador tijoriy funksiyalarda karyera izlayotgan mutaxassislar uchun qiziq bo‘lishi mumkin.

Medical Writing Manager - Pfizer UK Remote

Lead medical writing, quality control, and document strategy for Pfizer’s clinical and regulatory materials. Support accurate, evidence-based medical decision-making through robust documentation.

Tavsif

  • Lead or co-lead moderately complex projects while managing timelines and resources
  • Apply relevant expertise to support departmental activities
  • Resolve moderately complex issues independently within established policies
  • Complete assignments independently and seek guidance for unusual or complex issues
  • Review your work, incorporate feedback, and mentor colleagues through work reviews
  • Partner with project experts to shape document strategies and key messages
  • Ensure documents meet internal standards, are submission-ready, and stored correctly
  • Check document accuracy against source materials, including clinical regulatory documents and data
  • Lead author teams on complex projects
  • Conduct quality control reviews
  • Help train colleagues on quality standards and processes

Talablar

  • BA/BS or MBA/MS with some relevant experience; PhD/JD with any relevant experience; an associate degree with substantial relevant experience; or a high school diploma or equivalent with extensive relevant experience
  • Demonstrated pharmaceutical or biotechnology industry experience in document quality control and/or medical writing
  • Experience working with cross-functional study team members
  • Strong knowledge of medical terminology and clinical trials
  • Excellent interpersonal and communication abilities
  • Ability to plan, organize, prioritize, and complete multiple tasks within defined objectives
  • Proficiency with Microsoft Office applications
  • A master’s degree is highly desirable
  • Proficiency with software commonly used for data presentation and analysis
  • Strong problem-solving ability and independence in ambiguous situations
  • Experience leading or co-leading projects
  • Experience training colleagues on quality standards and processes
  • Experience using common AI tools, including generative technologies such as ChatGPT or Microsoft Copilot, to support problem-solving and productivity
  • Curiosity about improving outcomes with AI tools and understanding responsible AI practices, including risk management and ethical use

Imtiyozlar

  • Flexible workplace culture
  • Support for work-life harmony
  • Reasonable adjustments available during applications and throughout future careers
  • Employee training and development opportunities

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