
10,000+ employees
Founded 2010
BeOne Medicines is a global oncology company domiciled in Switzerland that is discovering and developing innovative treatments that are more affordable and accessible to cancer patients worldwide. With a portfolio spanning hematology and solid tumors, BeOne is expediting development of its diverse pipeline of novel therapeutics through its internal capabilities and collaborations. With a growing global team of more than 11,000 colleagues spanning six continents, the Company is committed to radically improving access to medicines for far more patients who need them.
🕒 May 29
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10,000+ employees
Founded 2010
BeOne Medicines is a global oncology company domiciled in Switzerland that is discovering and developing innovative treatments that are more affordable and accessible to cancer patients worldwide. With a portfolio spanning hematology and solid tumors, BeOne is expediting development of its diverse pipeline of novel therapeutics through its internal capabilities and collaborations. With a growing global team of more than 11,000 colleagues spanning six continents, the Company is committed to radically improving access to medicines for far more patients who need them.
• Responsible for providing expertise to support the development of clinical and regulatory documents • Mentor Medical Writers as needed • Manage document writing tasks and ensure compliance with regulatory guidelines • Navigate through uncertainties to manage timelines for multiple documents • Identify risks and develop mitigation plans • Contribute to process/tool optimization and establishment • Lead training programs and mentorship for Medical Writers
• Advanced degree (MS/PhD/PharmD/MD) in life science, pharmacy, medical, or health-related science preferred • BS with a minimum of 7 years of regulatory document writing experience, Masters with 5+, or PhD/PharmD/MD with 3+ years of regulatory document writing experience • Technical expertise in Microsoft Word, Adobe Acrobat, and electronic document management systems • Proficiency in Microsoft Outlook, Excel, and PowerPoint
• Medical • Dental • Vision • 401(k) • FSA/HSA • Life Insurance • Paid Time Off • Wellness
Apply Now🕒 May 27
Clinical Documentation Integrity Specialist reviewing medical records for compliance and accuracy. Collaborating with healthcare providers and educating on documentation best practices.
🇺🇸 United States – Remote
💰 $2M Grant on 2021-07
⏰ Full Time
🟡 Mid-level
🟠 Senior
🏥📝 Medical Writer
🦅 H1B Visa Sponsor
🕒 May 27
Clinical Documentation Integrity Analyst providing training and auditing to CDI Specialists for accurate medical documentation. Engaging with coding teams for quality outcomes and compliance in a health care setting.
🇺🇸 United States – Remote
💰 $2M Grant on 2021-07
⏰ Full Time
🟡 Mid-level
🟠 Senior
🏥📝 Medical Writer
🦅 H1B Visa Sponsor
🕒 May 27
Clinical Documentation Specialist ensuring accurate clinical documentation and provider education. Focused on improving risk profiles and billing processes through expert analysis.
🇺🇸 United States – Remote
💰 $2M Grant on 2021-07
⏰ Full Time
🟡 Mid-level
🟠 Senior
🏥📝 Medical Writer
🦅 H1B Visa Sponsor
🕒 May 22
Medical Writer II at Syneos Health leading writing projects and mentoring junior writers. Collaborating on complex medical documents while adhering to regulatory standards.
🕒 May 19
Senior Medical Writer developing and managing clinical study documents at Precision for Medicine. Ensuring compliance with regulatory guidelines and delivering high-quality outputs on time.
🇺🇸 United States – Remote
💵 $100.6k - $151k / year
💰 $75M Private Equity Round on 2015-12
⏰ Full Time
🟠 Senior
🏥📝 Medical Writer