
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
🗣️🇮🇹 Italian Required
Improve your chances of getting an interview by checking your resume score before you apply.

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 ensuring robust oversight of clinical trial compliance at the country and site level • Serve as the primary point of contact for country teams regarding GCP requirements • Analyze and confirm initial country and site-specific risks • Communicate identified country and site trends for continuous improvement • Conduct site compliance visits on identified high-risk sites
• Bachelor’s degree (BS/BA or equivalent) or higher in a scientific, medical or healthcare discipline • Minimum 5 years of progressive experience in clinical operations roles • Minimum 4 years’ experience in a GCP compliance or equivalent role (i.e. quality) is preferred • Experience in oncology global trials is preferred • Excellent English and Italian written and verbal communication
• Health insurance • Paid time off • Flexible work arrangements • Professional development opportunities
Apply Now🕒 May 27
Regulatory Affairs Specialist providing regulatory input for Global Surgical Solutions at Baxter. Collaborating with teams to ensure compliance and manage submissions for medical device products.
🕒 May 13
GRC Analyst supporting compliance and security operations at a leading SaaS provider. Managing audits, assessments, and ESG reporting while collaborating with cross-functional teams.