Senior Manager, Site Management

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Logo of BeOne Medicines

BeOne Medicines

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.

📋 Description

• Oversee clinical monitoring activities and CRA team's performance to ensure compliance with ICH-GCP, local regulations, and company SOPs • Allocate CRA resources and perform ongoing resource assessments • Ensure CRAs have the required level of monitoring knowledge and skills • Manage and address CRA performance and quality indicators • Strengthen site relationships • Review monitoring quality and resolve issues • Support study/site milestone delivery • Execute assessment visits and develop resolution strategies • Support site audits/inspections • Review and approve expenses related to CRA activities • Identify opportunities for cost-saving and efficiency • Provide mentorship and guidance to junior Clinical Research Managers • Lead and contribute to strategic initiatives and task forces • Perform recruiting and hiring activities, onboarding new team members • Assign tasks based on individual strengths and team objectives • Conduct regular performance evaluations and provide constructive feedback • Support team members in identifying and pursuing professional development opportunities

🎯 Requirements

• Bachelor’s degree or higher in a scientific or healthcare discipline, and advanced degrees preferred • Proficient in Microsoft Word, Excel, PowerPoint and Outlook • Fluent in written and verbal English • Minimum 7 years of industry experience in the pharmaceutical or CRO or relevant field • Minimum 4 years of People management or project management experience in progressive clinical research within the biotech, pharmaceutical sector, CRO industry or relevant field is preferred • Thorough understanding of the drug development process, including expert knowledge of international standards (ICH GCP) and health authority requirements • Understanding of all aspects of monitoring and trial execution, with previous experience as a CRA preferred • Excellent interpersonal skills, strong organizational and effective written and verbal communication skills. • Demonstrated team leadership experience. • Experience in Oncology is highly recommended

🏖️ Benefits

• Market competitive compensation package including performance-based annual bonus scheme • Company shares (generous welcome grant!) • In-house and external learning and development opportunities • Fantastic benefits program

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