
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.
🔥 2 minutes ago
🗣️🇫🇷 French Required
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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.
• Regional Clinical Compliance Country Manager is responsible for ensuring robust oversight of clinical trial compliance at the country and site level. • Provide expert guidance and interpretation of regulations and internal standards. • Analyze and confirm initial country and site-specific risks. • Communicates identified country and site trends for continuous improvement. • Identify high-risk sites using a structured, risk-based approach. • Conduct Site Compliance Visits on identified high-risk sites. • Support country teams in identifying, managing, and resolving compliance issues.
• Bachelor’s degree (BS/BA or equivalent) or higher in a scientific, medical or healthcare discipline • Minimum of 5 years of progressive experience in clinical operations roles • Minimum 4 years’ experience in a GCP compliance or equivalent role • Experience in oncology global trials is preferred. • Excellent English and French written and verbal communication • High attention to detail and quality orientation • Analytical and problem-solving skills • PC literacy required; MSOffice skills (Outlook, Word, Excel, PowerPoint)
• Travel: up to 20-30% travel
Apply Now🕒 June 30
Regulatory Affairs Specialist at Worldwide Clinical Trials navigating regulatory landscape and ensuring compliance in clinical trials. Collaborating with global teams for successful submissions and approvals.
🗣️🇫🇷 French Required
🕒 June 24
Compliance Engineer leading compliance programs and initiatives for a Digital Trust provider in Europe. Overseeing regulatory obligations and contributing to security efforts at Yousign.
🇫🇷 France – Remote
💵 €64k - €79k / year
💰 Series A on 2021-06
⏰ Full Time
🟡 Mid-level
🟠 Senior
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🗣️🇫🇷 French Required
🕒 May 27
Regulatory Compliance Officer responsible for enhancing compliance frameworks and managing regulatory requirements across multiple EU borders. Possibility to work fully remotely while based in France.
🗣️🇫🇷 French Required
🕒 November 4, 2025
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🗣️🇫🇷 French Required