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Senior Clinical Trials Data and Technology Analyst
Brown Medicine. Serve as a senior technical resource for clinical research applications, data integrations, analytics, and reporting solutions .
Posted 10/23/2026full-timeRemote • Rhode Island • United StatesSenior💰 $86,382 - $142,542 per yearWebsite
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in clinical research applications, data integration, and analytics, with a strong focus on application administration and workflow optimization. Proficient in developing reporting solutions and ensuring compliance with regulatory standards, particularly 21 CFR Part 11.
Highest-signal resume keywords
Clinical Trial Management SystemsData IntegrationApplication AdministrationReporting Solutions21 CFR Part 11 Compliance
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Data ManagementAnalyticsSQLPythonAPIsData PipelinesData VisualizationsMetrics DevelopmentWorkflow OptimizationTechnical Support
Soft Skills
Technical GuidanceMentoringCollaborationProblem SolvingAnalytical Skills
Tools & Technologies
OnCoreERegREDCapTrialConnXMicrosoft FabricPower BISnowflakeEpicWorkdayAdvarra Analytics
Industry Keywords
Clinical ResearchResearch InformaticsData GovernanceRegulatory RequirementsHealthcare Environment
Tech Stack
Tools & technologiesPythonSQL
About the role
Key responsibilities & impact- Serve as a senior technical resource for clinical research applications, data integrations, analytics, and reporting solutions
- Administer, configure, support, and optimize OnCore, eReg, REDCap, TrialConnX, Advarra Analytics, and related systems
- Provide advanced technical support for Microsoft Fabric, Power BI, Snowflake, and integrations with Epic, Workday, and other institutional systems
- Lead assigned technical, reporting, workflow improvement, validation, and enhancement projects
- Develop and maintain data pipelines, reporting solutions, dashboards, data visualizations, metrics, and key performance indicators
- Support research data marts, data models, and reporting environments
- Develop programs, scripts, APIs, data transformations, and automated workflows
- Troubleshoot application, data integrity, integration, and workflow issues
- Lead 21 CFR Part 11 validation activities, including validation plans, test scripts, traceability documentation, and change-control records
- Maintain application documentation, technical specifications, user support materials, and NetLearning training curricula
- Provide advanced end-user training, technical guidance, mentoring, and work direction
- Collaborate with CCRM, BHOCR, Information Services, research departments, and external vendors
- Facilitate technical collaboration between CCRM and BHOCR on oncology-specific requirements and OnCore solutions
Requirements
What you’ll need- Bachelor's degree in Information Systems, Computer Science, Health Informatics, Data Analytics, Clinical Research, or a related field required
- Minimum of seven (7) years of progressively responsible experience in research technology, application administration, data management, analytics, reporting, or research informatics within a healthcare, academic, or research environment
- Demonstrated experience supporting enterprise applications, developing reporting and analytics solutions, managing data integrations, and leading complex technical initiatives
- Advanced knowledge of clinical trial management systems, research applications, analytics, reporting platforms, and research informatics
- Demonstrated expertise in application administration, data integration, reporting, business intelligence, and workflow optimization within a clinical research environment
- Strong understanding of clinical trial operations, data governance, system validation, regulatory requirements, and 21 CFR Part 11 compliance principles
- Demonstrated ability to independently analyze complex technical and operational issues, develop practical solutions, manage multiple priorities, and provide technical guidance
- Proficiency with OnCore, eReg, REDCap, TrialConnX, Microsoft Fabric, Power BI, Snowflake, APIs, SQL, Python, and related technologies preferred
- Experience with clinical trial management systems, validated applications, and regulated research environments preferred
- Clinical research experience preferred
- Experience translating clinical, operational, and regulatory requirements into technology solutions highly desirable
- Occasional travel between Brown University Health locations may be required
- No driving required
Benefits
Comp & perks- Equal employment opportunities
- M-F 8:00am-5:00pm work schedule
- Day shift
- 8-hour daily schedule
- Remote work arrangement