Job summary The Senior Clinical Data Coder is primarily responsible for leading and overseeing activities related to the coding of clinical data across multiple ongoing studies. Responsibilities - Lead and perform accurate coding of medical terms and medications using MedDRA, WHO Drug, and internal conventions. - Oversee the setup of the coding module for assigned studies, ensuring correct configurations and workflows. - Define, document, and manage coding conventions and ensure consistent application across studies. - Act as the Lead Coder, coordinating coding activities across multiple studies simultaneously. - Manage coding priorities, balancing workload across timelines and studies. - Develop and maintain coding guidelines and synonym lists. - Provide input to the Coding section of Data Management Plans. - Oversee and perform dictionary up-versioning and related upgrade activities. - Validate and test coding setups, programming of coding reports, and related database checks. - Support data review activities and resolve data clarifications in a timely manner. - Provide mentorship and guidance to junior or back-up coders. - Actively contribute to process optimization, SOP development, and best practices in coding. - Maintain effective communication with Data Management Leads, CRAs, and other stakeholders. Requirements - Bachelor's degree or equivalent in pharmacy, life sciences, or a related field (medical/nursing background also acceptable). - Minimum of 5 years' relevant experience in clinical data coding within clinical trials or the pharmaceutical/CRO environment. - Thorough knowledge of medical terminology and medical dictionaries (MedDRA, WHO Drug). - Demonstrated experience with coding module setup, management of conventions, and prioritization of tasks across multiple studies. - Experience in query management and clinical data review. - Proven ability to manage multiple studies concurrently. - Excellent written and verbal English communication skills. - Strong organizational and analytical skills with high attention to detail. - Ability to lead within a global team environment, providing guidance to colleagues and ensuring deliverables are met. - Good knowledge of GCP and applicable Health Canada, FDA, and EMA regulations/guidelines. Benefits - Flexible work schedule / work schedule : - Home-based position - Ongoing learning and development Descripción del trabajo Lorem ipsum dolor sit amet , consectetur adipiscing elit. Nullam tempor vestibulum ex, eget consequat quam pellentesque vel. Etiam congue sed elit nec elementum. Morbi diam metus, rutrum id eleifend ac, porta in lectus. Sed scelerisque a augue et ornare. Donec lacinia nisi nec odio ultricies imperdiet. Morbi a dolor dignissim, tristique enim et, semper lacus. Morbi laoreet sollicitudin justo eget eleifend. Donec felis augue, accumsan in dapibus a, mattis sed ligula. Vestibulum at aliquet erat. Curabitur rhoncus urna vitae quam suscipit , at pulvinar turpis lacinia. Mauris magna sem, dignissim finibus fermentum ac, placerat at ex. Pellentesque aliquet, lorem pulvinar mollis ornare, orci turpis fermentum urna, non ullamcorper ligula enim a ante. Duis dolor est, consectetur ut sapien lacinia, tempor condimentum purus. Obtén acceso completo Accede a todos los puestos de alto nivel y consigue el trabajo de tus sueños. Inscríbete ahora