
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.
🔥 0 minutes ago
🗣️🇹🇷 Turkish 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.
• Ensure robust oversight of clinical trial compliance at the country and site level • Apply a risk-based approach to identify, evaluate, and manage compliance risks • Serve as the primary point of contact for country teams regarding GCP requirements • Analyze and confirm initial country and site-specific risks • 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 • PC literacy required; MSOffice skills (Outlook, Word, Excel, PowerPoint)
• Travel: up to 20-30% travel
Apply Now🕒 June 16
Regulatory and Start Up Specialist managing site activation for clinical trials in Turkey. Ensuring compliance with local and international regulations while coordinating with multiple stakeholders.
🗣️🇹🇷 Turkish Required
🕒 June 16
Regulatory and Start Up Specialist managing site activation for clinical trials at Precision Medicine Group. Overseeing timelines, quality, and regulatory submissions for successful trial initiation.
🗣️🇹🇷 Turkish Required