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POSITION TITLE: Student Worker Data MonitorLOCATION: Freiburg, Germany (Remote)This position reports to our Freiburg, Germany office (Heinrich-von-Stephan-Straße 5 | 79100 Freiburg Germany) and is fully remote with no expected travel. Who We Are: TriNetX connects healthcare organizations and researchers across the globe so they can see what’s happening in real patient populations—not guesses, not simulations.Our aim is simple and ambitious: Provide a clear path to trustworthy answers, whether your goal is to create promising new therapies, publish groundbreaking research, or improve health outcomes.We keep identifiable data where it belongs—inside more than 11,000+ clinical sites across 20+ countries—preserving security, provenance, and granularity. Our trusted partnerships with providers ensure high-fidelity data, and a properly governed linkage back to individual patients.At TriNetX, we enable life sciences, healthcare, and academic institutions to strengthen human health—with data you can trace, evidence you can defend, and answers you can trust. Who We Are Looking For: TriNetX, LLC has an immediate need for a Student Worker Monitor to join our team. TriNetX was founded on the idea that incorporating real-world data results in better clinical trial design, improves the site selection and patient recruitment process and generates real-world evidence (RWE) to advance the collective understanding of human health. This position requires a well-rounded individual who has demonstrated the ability to deliver results in a high-growth, dynamic, and fast-paced environment. We are looking for a highly motivated team player who brings a strong work ethic and analytical skills. What You Will Be Doing:Monitor and review clinical research data for accuracy, completeness, plausibility and consistencyEnsure compliance with study protocols and regulatory guidelinesIdentify and resolve data discrepancies or issues in a timely mannerVerifying the accuracy of all rules within the data capture system by entering test dataCommunicate with study sites and data managers to address data quality concernsReview data management plansAssist in the development and implementation of data quality assurance processesSupport in generating reports and presentations on data monitoring activities for internal and external stakeholdersResource planning and co-ordination of all monitors in consultation with head of project managementManage site administration activities and maintain recordsWork in interdisciplinary teams with (but not limited to) project management, data management, data operations, medical advisor, pharmacovigilanceSupport in training monitors (in conjunction with PM, DM and Medical Advisor)Support in setting up and testing electronic questionnaires /documentation formsSupport in pharmacovigilance related activitiesManagement of participants in medical data collection surveysAssisting adherence to quality standards, project requirements, and compliance regulations throughout the project lifecycleSupport in process optimization and revision of SOPs and work instructionsSupport in tasks related to other project management related activities What You Bring to TriNetX:Completed training in the healthcare sector; further certification as a monitor or similar is desirableExperience working in clinical research, data management, or related fieldStrong attention to detail and analytical skillsExcellent communication and interpersonal skillsAbility to work independently and as part of a teamKnowledge of electronic data capture systemsVery good knowledge of MS Office, especially in Word and ExcelKnowledge of regulatory guidelines and Good Clinical Practice (GCP) standardsYou convince through very structured work and a high degree of initiative, as well as a solution-oriented approachYou easily maintain a comprehensive understanding of project progress and status, with the ability to identify any potential issues or roadblocksTeam spirit, flexibility and excellent communication requiredAbility to work in a changing and agile environment with international collaborationsVery good written and spoken German and English skillsPreferred:Experience in oncology is of advantage but not a pre-requisiteLanguage skills additional to German and English are beneficial but not essential