9 часов назад
Medical Writing Manager
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Medical Writing Manager (Pharmaceutical and Clinical Research): Leading medical writing and document quality control for clinical and regulatory projects with an accent on scientifically robust, submission-ready documentation and cross-functional collaboration. Focus on developing document strategies, verifying evidence against clinical sources, leading author teams, and applying responsible AI tools to improve productivity.
Location: Remote within the United Kingdom or Canada
Company
is a pharmaceutical company focused on developing medicines and improving patient health outcomes through evidence-based medical decision support and digital transformation.
What you will do
- Lead or co-lead moderately complex medical writing and document quality projects.
- Collaborate with study team experts to develop document strategies and key messages.
- Lead author teams for complex projects and ensure documents meet internal standards and are submission-ready.
- Verify document accuracy against clinical regulatory documents, source materials, and data.
- Perform quality control reviews and contribute to training colleagues on quality standards and processes.
- Manage priorities independently, resolve moderately complex problems, and mentor colleagues through review and feedback.
Requirements
- BA/BS or MBA/MS with relevant experience; alternatively, a PhD/JD, Associate's degree with strong experience, or High School Diploma with extensive relevant experience.
- Demonstrated experience in document quality control and/or medical writing in the pharmaceutical or biotech industry.
- Experience interacting with cross-functional study team members.
- Solid understanding of medical terminology and clinical trials.
- Excellent interpersonal and communication skills, with the ability to plan, prioritize, and execute multiple tasks.
- Proficiency with Microsoft Office applications.
Nice to have
- Master's degree.
- Experience with software used for data presentation and analysis.
- Experience leading or co-leading projects and training colleagues on quality standards.
- Experience using generative AI tools such as ChatGPT or Microsoft Copilot, including responsible AI, risk management, and ethical use.
Culture & Benefits
- Flexible remote work arrangement within the United Kingdom or Canada.
- Workplace culture designed to support work-life harmony and flexibility.
- Patient-centric environment guided by courage, joy, equity, and excellence.
- Commitment to diversity, inclusion, accessibility, and reasonable workplace adjustments.
- Digital transformation initiatives using data, modelling, and automated solutions in drug discovery and development.
Hiring process
- Applications close on October 19, 2026.
- Candidate use of AI during recruitment is subject to 's AI-use guidelines.
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