About the role Motivated 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 responsibilities Provide ongoing support and maintenance for Acquire Clinical and its associated Medidata applications Manage 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 Clinical Assess the impact of new Medidata product releases on system availability, maintenance, security, and interfaces Drive and manage IT changes, including the update of computerized system validation (CSV) documentation and execution of IQ/OQ testing Implement system changes based on evolving user requirements and lead project management activities as needed Manage 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 experts Support the periodic review and continuous improvement of both Acquire Clinical and Trialgrid Ideal candidate You 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 field Proven hands-on experience with Medidata products (Imedidata, Cloud Admin, Rave, Coder) -mandatory Strong background in computerized system validation (CSV) and computerized system testing Experience in IT change management and access management Knowledge of project management and incident management (ITIL framework) is preferred Experience with Trialgrid is an advantage Minimum 3 years of experience in the pharmaceutical industry preferred Understanding of Clinical Development processes is considered a plus Soft skills: Fluent in English (spoken and written) Excellent technical writing and documentation skills Strong teamwork, communication, and collaboration abilities Organized, detail-oriented, and capable of working independently