[Hiring] Senior Clinical Trials Data and Technology Analyst @Brown Medicine

Role Description

The Senior Clinical Trials Data and Technology Analyst serves as a senior technical resource for the clinical research applications, data integrations, analytics, and reporting solutions managed by the Center for Clinical Research Management (CCRM). Working under the direction of the Manager of Clinical Trials Data and Technology, the Senior Analyst independently performs complex application administration, data management, reporting, validation, technical development, and system enhancement activities supporting Brown University Health’s clinical trial operations.

The Senior Analyst provides advanced technical support for:

• OnCore
• eReg
• REDCap
• TrialConnX
• Advarra Analytics
• Microsoft Fabric
• Power BI
• Snowflake

The position leads assigned technical projects, develops and maintains data pipelines and reporting solutions, troubleshoots complex application and data issues, and recommends workflow and system improvements.

Within the technology strategy, application governance, and priorities established by CCRM leadership, the Senior Analyst works closely with:

• Brown Health Office of Cancer Research (BHOCR)
• Clinical research departments
• Information Services
• External vendors

Serves as the primary technical resource for CCRM-supported clinical research applications and research informatics solutions.

Given BHOCR’s significant operational experience with and historical investment in OnCore, the Senior Analyst facilitates ongoing technical collaboration between CCRM and BHOCR. This includes:

• Gathering oncology-specific requirements
• Evaluating workflow impacts
• Supporting testing
• Helping develop solutions that address both institutional and oncology research needs

In addition to our values, all employees are expected to demonstrate the core Success Factors which include:

• Instill Trust and Value Differences
• Patient and Community Focus and Collaborate

Qualifications

• 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 to users and team members.
• Proficiency with clinical research applications and analytics tools, including OnCore, eReg, REDCap, TrialConnX, Microsoft Fabric, Power BI, Snowflake, APIs, SQL, Python, and related technologies preferred.

Requirements

• 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.
• Experience with clinical trial management systems, validated applications, and regulated research environments preferred.
• Clinical research experience, including experience as a clinical research coordinator, nurse, regulatory specialist, research data manager, or other research operations role, is preferred.
• Experience translating clinical, operational, and regulatory requirements into technology solutions supporting clinical research workflows is highly desirable.

Work Environment and Physical Requirements

• Normal office environment with frequent computer use and regular interaction with clinical research, operational, and technical personnel.
• Occasional travel between Brown University Health locations may be required to support system implementations, training, or project activities.

Independent Action

• Exercises a high degree of independent judgment in the administration, configuration, support, and optimization of clinical research applications, reporting platforms, and data integrations.
• Independently evaluates technical issues, develops solutions, leads assigned projects, and recommends system and workflow improvements.
• Works within established CCRM governance, policies, priorities, and technology standards while collaborating with BHOCR and other key stakeholders to support clinical research technology initiatives.

Supervisory Responsibility

• Provides technical leadership, mentoring, training, and work direction to analysts, coordinators, and other research personnel involved in clinical research technology and reporting activities.
• May lead project teams and coordinate assigned technical initiatives. Does not have direct responsibility for hiring, performance management, compensation, or disciplinary actions.

Pay Range

$86,382.40-$142,542.40

EEO Statement

Brown University Health is committed to providing equal employment opportunities and maintaining a work environment free from all forms of unlawful discrimination and harassment.

Location

Remote-Rhode Island - N/A Providence, Rhode Island 02901

Work Type

M-F 8:00am-5:00pm

Work Shift

Day

Daily Hours

8 hours

Driving Required

No