
10,000+ employees
Founded 2010
🧬 Biotechnology
🏥 Healthcare
💊 Pharmaceuticals
Biotechnology • Healthcare • Pharmaceuticals
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 the 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.
🕒 August 4
🇩🇪 Germany – Remote
💵 €83.4k - €104.3k / year
⏰ Full Time
🟡 Mid-level
🟠 Senior
🧪 Clinical Research
👻 Ghost score 2%
🗣️🇩🇪 German Required
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10,000+ employees
Founded 2010
🧬 Biotechnology
🏥 Healthcare
💊 Pharmaceuticals
Biotechnology • Healthcare • Pharmaceuticals
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 the 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.
• Act as line manager for Clinical Research Associates and trial monitoring staff • Plan, assign, and direct work; assess performance and guide professional development • Participate in hiring selection and allocate staff to clinical research projects • Manage study start-up and trial monitoring staff • Onboard and train new employees and oversee training plans • Manage the quality of assigned staff’s clinical work through regular review and evaluation • Provide country-specific study start-up expertise to study teams • Review study start-up documents, drug labels, informed consent forms, and related materials • Develop and review site-specific recruitment materials and tools • Collaborate with regional operations managers and clinical sites on submissions, TMF completeness, site activation, enrolment, and inspection readiness • Contribute to feasibility, site identification, selection, and evaluation • Perform accompanied CRA visits and assess performance • Review visit reports, resolve issues, and communicate significant risks and proposed actions • Monitor workload and quality metrics through regular review and reporting • Identify site issues, propose CAPAs, identify gaps, and pursue operating improvements • Contribute to Clinical Operations strategy and performance against key metrics
• Bachelor’s degree (or equivalent) or higher in a scientific, medical, or healthcare discipline • Minimum 5–7 years of progressive experience in clinical operations within the biotech/pharmaceutical sector • Prior clinical trial experience, including management or leadership experience • Oncology experience highly recommended • Preferably at least 2 years of line management experience in the pharmaceutical or CRO industry • Ability to work independently and handle multiple priorities in a fast-paced environment • Excellent interpersonal and strong organizational skills • Fluent in German and English, written and spoken • Efficient in Microsoft Word, Excel, MS Project, MS PowerPoint, and Outlook • Willingness to travel up to 30–40%
• Full-time employment • Equal opportunity employment
Apply Now🕒 August 4
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