Senior Clinical Trial Analytics Monitor I

**This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Senior Clinical Trial Analytics Monitor I based in Canada.** This role offers the opportunity to support the advancement of clinical research through innovative analytics, reporting solutions, and technology-driven processes. You will work at the intersection of clinical operations, data management, statistics, and technology teams to transform complex clinical data into meaningful insights. The position focuses on designing scalable reporting solutions, improving data visibility, and enabling informed decision-making across clinical programs. You will contribute to the development and optimization of clinical trial technology platforms while ensuring quality, accuracy, and usability. Working in a collaborative and global research environment, you will partner with internal teams and external stakeholders to deliver impactful solutions. This role is ideal for an analytical professional passionate about healthcare innovation, business intelligence, and improving clinical trial outcomes. ### Accountabilities: As a Senior Clinical Trial Analytics Monitor I, you will be responsible for leading analytics initiatives, supporting clinical technology solutions, and ensuring reliable reporting capabilities across clinical research programs. Your responsibilities will include: - Collaborating with stakeholders across clinical operations, medical affairs, data management, statistics, and project management teams to gather reporting requirements and align on business needs. - Acting as a connection point between technical teams and external/internal stakeholders to ensure reporting solutions are accurate, relevant, and actionable. - Leading the collection, documentation, and standardization of reporting requirements to identify opportunities for improved consistency and efficiency. - Defining and maintaining standardized metrics, key performance indicators (KPIs), and business definitions across reporting solutions. - Designing, developing, and maintaining interactive dashboards and reports using business intelligence tools such as Spotfire and clinical data reporting platforms. - Validating data sources, applying transformations, performing quality checks, and ensuring accuracy and consistency across reports. - Partnering with technical teams to troubleshoot data integration issues and improve reporting functionality. - Supporting the creation and maintenance of BI standards, documentation practices, report repositories, and governance processes. - Monitoring performance indicators, identifying trends and anomalies, and providing insights to support data-driven decisions. - Supporting clinical technology start-up activities, including requirements documentation, testing plans, user acceptance testing, application demonstrations, and training sessions. - Creating and reviewing technical documentation, user guides, and study-specific materials to support effective application use. - Contributing to quality assurance processes, product development initiatives, capability improvements, and business development activities. - Providing analytical support and recommendations to leadership teams on clinical technology and reporting initiatives. ## Requirements: The ideal candidate combines clinical research expertise, analytics experience, technical proficiency, and strong communication skills to support complex clinical technology environments. Required qualifications and experience include: - Bachelor’s degree in health sciences, physical or biological sciences, computer science, or a related field. - Minimum of 5 years of experience in clinical research data analytics and business intelligence reporting implementation. - 4+ years of experience with programming languages such as SQL, PL/SQL, R, Python, or SAS. - Experience developing and maintaining enterprise clinical data standards and reporting solutions. - Ex…