
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.
10,000+ employees
Founded 2010
November 15
đşđ¸ United States â Remote
đľ $105.8k - $140.8k / year
â° Full Time
đ Senior
đŹ Research Analyst

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.
10,000+ employees
Founded 2010
⢠Perform and coordinate assigned aspects of the clinical monitoring process in accordance with GCPs and SOPs to assess the safety and efficacy of investigational products and/or medical devices ⢠Conduct site visits to determine protocol and regulatory compliance, and prepare required documentation ⢠Develop collaborative relationships with investigative sites, and study vendors ⢠Track enrollment status reports to ensure study sites stay on track to meet enrollment goals ⢠Track study-specific status reports to ensure all required information regarding site issues, deviations, and CRF status are kept current by the monitoring team ⢠Serve as mentor/trainer for less experienced CRAs ⢠Collaborate with CST and clinical study sites to ensure timely delivery of study milestones
⢠Minimum of 4-6 years of relevant Clinical Operations experience ⢠Minimum of 3-4 years of (CRA) monitoring experience in the pharmaceutical or CRO Industry ⢠Excellent communication and interpersonal skills ⢠Excellent organizational skills and ability to prioritize and multi-task ⢠BS/BA in a relevant scientific discipline
⢠Medical ⢠Dental ⢠Vision ⢠401(k) ⢠FSA/HSA ⢠Life Insurance ⢠Paid Time Off ⢠Wellness
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