Site Solutions Executive, Clinical Trials
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Coordinate clinical trial compliance, documentation, and patient procedures at Premier Research’s Bangalore site. Support investigators, sponsors, and CROs throughout study delivery.
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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 or Canada Remote)
Lead medical document strategy, quality control, and author teams for Pfizer. This full-time role is remote in the United Kingdom or Canada.
Tavsif
- Lead or co-lead moderately complex projects while managing timelines and resources
- Apply professional expertise to support departmental priorities
- 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 subject-matter experts to shape document strategies and key messages
- Ensure documents meet internal standards, are submission-ready, and properly archived
- Validate document accuracy against source materials, including clinical regulatory records and data
- Lead author teams on complex projects
- Conduct quality control reviews
- Support colleague training on quality standards and processes
Talablar
- Bachelor’s degree 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 medical writing or document quality-control experience in the pharmaceutical or biotechnology industry
- Experience collaborating with cross-functional study team members
- Strong knowledge of medical terminology and clinical trials
- Excellent interpersonal and written and verbal communication skills
- Ability to plan, organize, prioritize, and complete multiple tasks against defined objectives
- Proficiency with Microsoft Office applications
- Master’s degree preferred
- 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
- Interest in using AI to improve outcomes and understanding of responsible AI practices, including risk management and ethical use
Imtiyozlar
- Flexible workplace culture designed to support work-life harmony
- Reasonable accommodations for applicants and employees with disabilities
- Commitment to equal employment opportunity and an inclusive workplace
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