Main ResponsibilitiesConducting all tasks regarding clinical data management with AO ITC, such as:Set up and validation of clinical study databases in the field of trauma and orthopedicsSet up, implement and oversee Data Management Plans and Data Validation PlansSupport and supervision of data cleaning and data clarification activitiesData base user management for clinical research projectsManagement and maintenance of the AO ITC case report form template libraryMaintenance and further development of Clinical Data Management SOPsLine management optionalIn General:Functional lead of the Clinical Data Management team, including resource planning, cross-functional communication and leading the Data Management Jam SessionsSupporting the Head of Clinical Operations in strategical decisions related to the Clinical Data Management team (e.g., development of budgets, project prioritization, further education goals)Main RequirementsEducation:Degree in Information Technology, Computer Science, Life Sciences, or related field. Equivalent education or certification in clinical data management or database development will also be considered.Basic level of medical knowledge of advantageJob Specification:Extensive experience with data management in clinical research, particularly in utilizing electronic data capture (EDC) systems such as REDCap Academic, REDCap Cloud, and MedidataExperience in managing the full data lifecycle from data collection to final reporting, ensuring accuracy, completeness, and consistency. Ability to develop and maintain databases, including designing and implementing case report forms, queries, and reports. Able to lead the configuration, design, and administration of REDCap and Medidata platforms for clinical trials or research projects. Experienced in implementing study-specific case report forms, including programming automated data validation rules and range checks.Used to designing, implementing, and monitoring data validation protocols to ensure data integrity and regulatory compliance. Able to conduct thorough data quality checks, consistency checks, and identify discrepancies between data sources.Familiarity with data privacy regulations and guidelines, such as GDPR and HIPAA, in the context of clinical data handlingProficient knowledge of MS Office work package, especially MS Excel, project management software (e.g., MS Project, JIRA) and clinical data management toolsExpertise in designing, setting up, and managing clinical databases adhering to global clinical data standards, such as CDISC, including CDASH and SDTM standardsDemonstrated ability to manage complex clinical data management workflows with strong organizational, planning, and follow-up capabilitiesAttention to detail and reliabilityCollaborative and team-oriented with the ability to work cross-functionallyFlexibility and customer-oriented mindsetStrong written and oral communication in English, German skills are of advantageAn interesting and varied job in an exciting and innovative organizationThe opportunity to be part of a highly committed international teamModern infrastructureHigh degree of flexibility regarding working hours and location (depending on operational requirements)Generous pagacke of social benefits, including supplementary vacation days and pension scheme contributionsInternal skills training opportunities and support for continued education