Associate Clinical Data Manager

Vor 7 Tagen


City of Melbourne, Österreich Novotech Vollzeit

About the Role Associate Clinical Data Manager - RTSM is responsible for planning, conducting and managing all aspects of data management for a clinical trial according to client specifications, protocol, project plan, Data Management Plan, relevant GCDMP guidelines, regulatory requirements and SOPs. Responsibilities Develop and maintain Trial Supply Management (TSM) specifications to ensure accurate system configuration and compliance. Serve as the primary RTSM support for sites, Project Managers, and CRAs, providing guidance and resolving system-related issues. Perform comprehensive data management tasks including data review, query management, external data reconciliation. Determine project feasibility from a data management perspective. Understand the requirements of the project agreement and scope to ensure that Novotech performs these services as required. Design and review of database structure, validation rules and consistency checks. Operate Clinical Data Management software for data entry of clinical trial results. Experience and Qualifications Graduate in a clinical or life sciences related field. At least three to six years experience working in a Clinical Data Associate (or equivalent) role in a pharmaceutical industry or related role. Must have Randomization and Trial Supply Management experience. Novotech is committed to gender equality and an inclusive work environment where everyone is treated fairly and with respect. We offer flexible working options, paid parental leave for both parents, flexible leave entitlements, wellness programs and ongoing development programs. We welcome applicants including those who identify as LGBTIQ+, have a disability or have caring responsibilities. We are a Circle Back Initiative Employer and commit to respond to every application. We look forward to talking to you about working at Novotech. Location: Melbourne, Victoria, Australia #J-18808-Ljbffr



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