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BeOne Medicines is a Switzerland-domiciled global oncology company focused on discovering and developing innovative cancer treatments designed to improve affordability and access. Its portfolio covers hematologic cancers and solid tumors, supported by an expanding pipeline of novel therapeutics advanced through in-house capabilities and external collaborations. With more than 11,000 colleagues across six continents, BeOne Medicines is working to broaden access to medicines for patients worldwide.
Junior Quality Control Specialist, Medical Writing — BeOne Medicines (Remote, United States)
BeOne Medicines is seeking a junior Quality Control Specialist to review and refine clinical and regulatory documents. The role supports scientific accuracy, regulatory compliance, and submission-ready quality across global medical writing projects.
Description
- Manage assigned quality-control reviews for clinical and regulatory documents
- Conduct copyediting, proofreading, cross-referencing, fact-checking, data verification, and broader quality evaluations
- Review study reports, clinical study protocols and amendments, investigator brochures, INDs, NDAs, MAAs, manuscripts, abstracts, posters, briefing documents, health-authority responses, and narratives
- Confirm documents follow internal standards, Global Medical Writing conventions, applicable regulatory guidance, and project schedules
- Keep related documents consistent while checking hyperlinks, sources, formatting, grammar, syntax, and scientific content
- Balance multiple projects and deliver QC reviews under tight deadlines and changing priorities
- Coordinate with Medical Writers on expectations, milestones, and deliverables
- Support discussions about team direction and strategy
- Develop collaborative relationships with internal departments
- Take part in training on medical writing, medical terminology, drug and biologics development, and document types
Requirements
- Strong written and verbal English communication skills
- Experience performing medical writing quality-control reviews for pharmaceutical regulatory documents or technical editing in a comparable industry
- Familiarity with drug and biologics development and FDA and ICH regulatory submission requirements is preferred
- Technical proficiency with Microsoft Word, Outlook, Excel, PowerPoint, and Adobe Acrobat
- Ability to work effectively in Microsoft Windows
- Familiarity with SharePoint and Veeva Vault is advantageous
- Bachelor’s degree in any field
- At least one year of relevant industry experience as a QC editor or specialist, medical writer, or technical copyeditor
Benefits
- Eligibility for an annual bonus plan in non-commercial roles
- Eligibility for an incentive compensation plan in commercial roles
- Discretionary equity award opportunities
- Optional participation in the Employee Stock Purchase Plan
- Medical insurance
- Dental insurance
- Vision insurance
- 401(k) plan
- FSA and HSA options
- Life insurance
- Paid time off
- Wellness benefits
- Remote work or the option to work from a BeOne global office
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