BeOne Medicines
10,000+ employees
Founded 2010
𧏠Biotechnology
đĽ Healthcare
đ 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.
Senior Clinical Research Associate
đĽ 4 minutes ago
đŁď¸đšđˇ Turkish Required
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BeOne Medicines
10,000+ employees
Founded 2010
𧏠Biotechnology
đĽ Healthcare
đ 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.
đ Description
⢠Execute clinical monitoring activities at clinical trial sites ⢠Monitor clinical trials in accordance with ICH guidelines and GCP ⢠Perform monitoring activities related to site selection, initiation, and conduct of trials ⢠Collaborate with Country and Regional Clinical Study Teams ⢠Provide protocol and related study training to assigned sites ⢠Conduct monitoring visits per monitoring plan and applicable SOPs ⢠Ensure inspection readiness of the study and sites ⢠Manage sites and site performance by tracking regulatory submissions and data query resolution ⢠Evaluate the quality and integrity of site practices ⢠Mentor junior staff
đŻ Requirements
⢠BS in a scientific or healthcare discipline preferred ⢠At least 3 - 5 years of monitoring experience ⢠Advanced knowledge of applicable clinical research regulatory requirements ⢠Excellent communication and interpersonal skills ⢠Experience in oncology/onco-hematology global trials preferred ⢠Excellent organizational and problem-solving skills ⢠Written and verbal communication skills in English and Turkish ⢠Proficient in Microsoft Word, Excel, PowerPoint, and Outlook
đď¸ Benefits
⢠Competitive salary ⢠Health insurance ⢠Paid time off ⢠Professional development opportunities
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