Reporting Programmer (Clinical Data)

The Reporting Programmer is responsible for ensuring that the reporting environment meets the needs of Clinical Study Teams by gathering requirements, analyzing reporting requests, coordinating with business and technical stakeholders, and delivering high-quality reports and dashboards that support clinical decision-making. Requirements Gathering & Business Analysis Collaborate with Study Management, Clinical Data Management, and other stakeholders to identify reporting needs. Collect, analyze, and document requests for new reports, dashboards, enhancements, and modifications. Understand the business objectives and intended use of each reporting request. Identify target users and define the decision-making processes supported by reports. Assess existing reporting solutions before initiating new developments. Define report scope, timelines, study population, data sources, refresh frequency, and delivery methods. Stakeholder Management & Coordination Facilitate requirement-gathering workshops and meetings with business stakeholders. Act as the interface between business teams and technical experts. Ensure proper communication and alignment between stakeholders throughout the project lifecycle. Maintain end-to-end traceability of reporting requests from submission through implementation. Reporting Development & Documentation Produce detailed report specifications and functional requirements. Support the implementation and enhancement of reports and dashboards. Maintain reporting documentation and ensure consistency across deliverables. Prepare and distribute meeting minutes and follow-up action plans. Ensure delivered reports meet business expectations and quality standards. Master's Degree in Science, Engineering, Computer Science, Data Management, or a related field. 2 to 5 years of experience in clinical reporting, clinical data management, or a related environment. Technical Skills Experience in clinical trial reporting environments. Knowledge of clinical research processes and clinical trial data management. Understanding of Computerized System Validation (CSV) principles. Experience in business requirements gathering and documentation. Ability to understand complex system architectures and data flows. Previous experience with Oracle solutions is highly desirable. Knowledge of reporting and dashboarding tools is an advantage. Soft Skills Excellent communication and listening skills. Strong analytical and problem-solving abilities. Solution-oriented mindset. Strong organizational and stakeholder management skills. Ability to work in cross-functional and international environments. Open-mindedness and adaptability.