Senior Global Study Management Associate

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BeOne Medicines

WebsiteLinkedInAll Job Openings

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

• Supports the Global Clinical Study Manager in global study delivery and ensures that delegated components of clinical studies are executed to expected and specified quality standards, within timelines and budget • Supports the alignment of study goals with clinical operations goals and objectives under direction of the Global Clinical Study Manager • Supports study vendor management in addition to other study management activities assigned • Supports the Global Clinical Study Manager with the organization and logistics for cross-functional Clinical Study Team (CST) meetings • Establishes good collaboration with the Global Clinical Study Manager, Regional Clinical Trial Management Associates and other key stakeholders globally and regionally • Knowledgeable of clinical study operations, including interpretation and implementation of regulatory and ICH-GCP guidelines • Builds solid knowledge of global clinical trials operations under the guidance of the Global Clinical Study Manager • Actively contributes to GSMA task force initiatives and cross functional projects within scope, supporting process improvement, standardization, and implementation activities as required • Creates and maintains study-level SharePoint and CST distribution lists • Sets up the study in the appropriate systems e.g. eTMF, CTMS etc and makes sure study-level information is kept up to date • Ensures system access is granted and managed appropriately across the study life cycle, supports user account management for systems used in study • Supports the development of various study plans • May assist in the review of study-related documents as delegated by the Global Clinical Study Manager (e.g., Clinical protocols, Informed consent forms, Investigator Brochures, Pharmacy Manual, Monitoring Plan, Laboratory Manual, Patient Diary, Pharmacy Manual, Case Report Form (CRFs), CRF Completion Guidelines and other relevant study plans and charters) • Organizes study-specific investigator meetings under supervision of the Global Clinical Study Manager • Might support the creation and review of site feasibility assessments required for study participation • Manages and tracks key study deliverables such as screening, enrollment, biological samples and images, data flow and protocol deviations in relevant systems in collaboration with Regional Clinical Trial Management Associates • Prepares metrics and updates to key deliverables for management as per information available in relevant systems • Supports the preparation of a study newsletter and other correspondence related to the study conduct (e.g. frequently asked questions, lessons learned) in collaboration with the study team • Supports the TMF specialist with study-level TMF creation and, as required, maintains the study-level TMF, including regular review and QC of TMF documents as per the study TMF QC plan • Supports the Global Clinical Study Manager with study drug forecasts and overall study drug supply activities in collaboration with Global Clinical Supplies • Supports the overall data cleaning activities and contributes to the follow-up of outstanding information • Supports the Global Clinical Study Manager with planning and execution of the Clinical Study Report • Supports the identification of operational risks and issues and works with the Global Clinical Study Manager to recommend solutions for discussion with appropriate team leadership • Learns and shares best practices in clinical operations methodologies, systems and processes with an emphasis on quality and compliance • Suggest improvements to enhance efficiency and the quality of the work performed on assigned projects • Might support the development of global study tools, working instructions and SOPs • Supports selection and set-up of vendors for global outsourced activities • Supports study budget management activities with responsibility for PO setup and payment invoice tracking across all study lifecycles.

🎯 Requirements

• Bachelor or higher degree in a scientific or healthcare discipline*, higher degree preferred. • Proficiency in MS Office Suite, including Excel, PowerPoint, and Project etc. • Knowledge of clinical operations methodologies, understanding of operational aspects of clinical study processes • 3 or more years of experience in clinical research within Biotech, Pharma or CRO industry

🏖️ 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