 
        About the roleMotivated professionals make a difference - not only for themselves but also for our customers.We are seeking an enthusiastic IT Solution Expert - Clinical Data Acquisition Systems to join our team. In this role, you will be responsible for supporting and maintaining the primary clinical data acquisition platform, Acquire Clinical, which includes a suite of Medidata 15 products such as Imedidata, Rave, and Coder.Key responsibilitiesProvide ongoing support and maintenance for Acquire Clinical and its associated Medidata applicationsManage and ensure the successful transition to Cloud Admin and Coder+Support and maintain Trialgrid, the quality tool used to verify clinical study builds for Acquire ClinicalAssess the impact of new Medidata product releases on system availability, maintenance, security, and interfacesDrive and manage IT changes, including the update of computerized system validation (CSV) documentation and execution of IQ/OQ testingImplement system changes based on evolving user requirements and lead project management activities as neededManage access control for specific user roles within Acquire Clinical (granting and revoking access)Handle incident management in close collaboration with Medidata and internal subject matter expertsSupport the periodic review and continuous improvement of both Acquire Clinical and TrialgridIdeal candidateYou are a structured, analytical, and proactive professional with a strong understanding of clinical data systems, validation processes, and regulated environments. You can effectively manage both technical and organizational aspects of IT system support in a pharmaceutical context.Required qualifications:Bachelor's degree (minimum) in Computer Science or a related fieldProven hands-on experience with Medidata products (Imedidata, Cloud Admin, Rave, Coder) -mandatoryStrong background in computerized system validation (CSV) and computerized system testingExperience in IT change management and access managementKnowledge of project management and incident management (ITIL framework) is preferredExperience with Trialgrid is an advantageMinimum 3 years of experience in the pharmaceutical industry preferredUnderstanding of Clinical Development processes is considered a plusSoft skills:Fluent in English (spoken and written)Excellent technical writing and documentation skillsStrong teamwork, communication, and collaboration abilitiesOrganized, detail-oriented, and capable of working independently