BeOne Medicines
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.
Principal Medical Writer
🕒 May 29
📊 Check your resume score for this job
Improve your chances of getting an interview by checking your resume score before you apply.
BeOne Medicines
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.
📋 Description
• Provides expertise to support the development of high-quality clinical and regulatory documents • Manages assigned writing tasks ensuring adherence to regulatory guidelines • Navigates uncertainties to develop and manage timelines of individual and multiple documents • Identifies needs for process/tool optimization and proposes solutions • Leads development of new training programs for junior MWs
🎯 Requirements
• An advanced degree (MS/PhD/PharmD/MD) in life science, pharmacy, medical, or health-related science is preferred • Bachelor's with 5+, MS with a minimum of 4+ years of regulatory document writing (or equivalent) experience, or PhD/PharmD/MD with a minimum of 2+ years of regulatory document writing (or equivalent) experience • Technical expertise in Microsoft Word, Adobe Acrobat, and electronic document management systems • Proficiency in Microsoft Outlook, Excel, and PowerPoint
🏖️ Benefits
• Medical • Dental • Vision • 401(k) • FSA/HSA • Life Insurance • Paid Time Off • Wellness
Apply NowSimilar Jobs
🕒 May 26
Clinical Documentation Improvement Specialist responsible for enhancing the quality of inpatient medical record documentation. Collaborating with medical staff and ensuring compliance with coding practices and regulations.
🕒 May 22
Director of Clinical Documentation Improvement overseeing CDI functions in healthcare revenue cycle organization. Ensures documentation integrity, coding accuracy, quality outcomes, and regulatory compliance.
🕒 May 20
GeneDx
1001 - 5000
Principal Medical Writer developing scientific publications for GeneDx. Collaborating with cross-functional teams to create high-quality content in the clinical genomics field.
🕒 May 6
RN Educator enhancing clinical documentation integrity at Denver Health, requiring strong nursing and CDI experience. Focus on education and training for improved documentation quality and compliance.
🇺🇸 United States – Remote
💵 $85.6k - $132.6k / year
⏰ Full Time
🟠 Senior
🔴 Lead
🏥📝 Medical Writer
🦅 H1B Visa Sponsor
🕒 April 30
4D Molecular Therapeutics
51 - 200
Principal Medical Writer at 4D Molecular Therapeutics supporting gene therapy for retinal vascular diseases. Responsible for high-quality clinical and regulatory document development in late-stage clinical trials.
🇺🇸 United States – Remote
💵 $180k - $202k / year
⏰ Full Time
🔴 Lead
🏥📝 Medical Writer
🦅 H1B Visa Sponsor
