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Spotfire Jobs in Raleigh, NC (NOW HIRING)

UCB

Digital Lead, Clinical Analytics

Raleigh, NC

$125K - $165K/yr

Ability to use analytical environments like PowerBI, Spotfire, Qlik to discover insights Preferred: * Experience with key technology services providers and best practices of the industry.

UCB

Digital Lead, Clinical Analytics

Raleigh, NC · On-site

$125K - $165K/yr

Ability to use analytical environments like PowerBI, Spotfire, Qlik to discover insights Preferred: * Experience with key technology services providers and best practices of the industry.

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Spotfire information

See Raleigh, NC salary details

$40.3K

$80.3K

$128.3K

How much do spotfire jobs pay per year?

As of Aug 27, 2026, the average yearly pay for spotfire in Raleigh, NC is $80,325.00, according to ZipRecruiter salary data. Most workers in this role earn between $63,700.00 and $92,300.00 per year, depending on experience, location, and employer.

What is a Spotfire?

A Spotfire job typically involves working with TIBCO Spotfire, a powerful data visualization and business intelligence tool. Professionals in this role use Spotfire to analyze complex datasets, create interactive dashboards, and generate insights for business decision-making. Common responsibilities include data integration, scripting with IronPython or R, and optimizing data visualizations for performance and usability. Spotfire jobs are often found in industries like healthcare, finance, and energy, where data-driven insights are crucial for operations. Strong SQL, data modeling, and analytical skills are usually required for success in this role.

What does a Spotfire do?

A typical day for a Spotfire professional involves gathering data requirements from stakeholders, developing interactive dashboards and reports using TIBCO Spotfire, and performing data analysis to identify business trends and insights. You may also be responsible for maintaining data integrity, troubleshooting data issues, and providing support to end-users. Collaboration is often required with data engineers, business analysts, and other departments to ensure seamless data integration and actionable reporting. Spotfire specialists are frequently involved in training others in the organization on how to use dashboards and interpret data visualizations. This role provides a dynamic work environment with plenty of opportunities to have a direct impact on strategic business decisions.

What are the key skills and qualifications needed to thrive in the Spotfire position, and why are they important?

To excel as a Spotfire developer or analyst, you need strong data visualization, analytical, and problem-solving skills, typically backed by experience with business intelligence tools and a degree in a related field. Proficiency in TIBCO Spotfire software, data modeling, SQL, and potentially certifications like TIBCO Certified Professional are highly valued. Excellent communication, teamwork, and an ability to translate complex data insights to non-technical audiences are essential soft skills. These competencies enable you to extract meaningful insights from data and drive informed decision-making within organizations.

What are popular job titles related to Spotfire jobs in Raleigh, NC?

For Spotfire jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Spotfire jobs in Raleigh, NC look for?

The top searched job categories for Spotfire jobs in Raleigh, NC are:

What cities near Raleigh, NC are hiring for Spotfire jobs?

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Infographic showing various Spotfire job openings in Raleigh, NC as of August 2026, with employment types broken down into 100% Full Time. Highlights an 83% In-person, and 17% Remote job distribution, with an average salary of $80,325 per year, or $38.6 per hour.

Senior/Principal Clinical Programmer

Raleigh, NC • On-site, Remote

Biodata Partners, Inc.
See more jobs at Biodata Partners, Inc.external

Full-time

Re-posted 4 days ago

Job description

Job Title: Principal Clinical Programmer
Job Code: CDM0016
Department Name: Clinical Data Management
Reports to Title: Manager or above
Job Summary:
The Principal Clinical Programmer is a member of the Data Management team and serves as a subject matter expert for Clinical Data Programming, Reporting, Process, and technology. Accountable for the quality and delivery of the Data Management programming, reporting and visualization, standard, and exception data listings across studies. Scope of work includes oversight and expertise in the design, development, and validation of programs, standard and adhoc reports, standard and exception data listings, and visualizations to support ongoing data review activities, achieve critical study milestones, and gain data insights into our clinical studies. The position requires good understanding of programming methods and techniques, critical thinking, and complex problem-solving skills. This position will require strong collaboration in working with other members of the Biostatistics and Data Management, external CRO partners, and other stakeholders.
Responsibilities:
  • Serve as a subject matter expert and provide expertise for Database programming, Reporting, and Technology and optimize the use of J-Review, ETL, SAS tools, and others to support business needs.
  • Manage the quality of the data management clinical database programming deliverables including edit checks programming, complex reports, and listings; patient profiles, subject narratives, exception listings, dose modification reports, and other adhoc reports using JReview & SAS as part of standard data validation and reporting package for clinical studies.
  • Develop and/or provide oversight on the programming specifications for the data validation and reporting deliverables; code, test, and document deliverables conforming to programming standards, data quality and governance, and validation policies.
  • Partner with internal and external stakeholders to ensure timely delivery of data management programming, EDC database, external data, data management programming of reports and listings including the use of visualization tools.
  • Design and develop macros, applications, and other utilities to expedite JReview/SAS programming activities.
  • Develop standard programs, templates, reports, data listings, discrepancy reports, and patient profiles to facilitate in the ongoing review of clinical data during study conduct and study closeout.
  • Build, test, and scale-up programs for data validation derivation procedures, data reports, listings, and SAS on Demand relational database extracts for operational use, identification of data outliers, quality inconsistencies, and preparation for analysis.
  • Provide technical guidance and direct programming tasks for Medical Coding activities.
  • Provide Clinical Programming expertise and support for critical and time-sensitive study milestones including interim analysis, and database lock activities.
  • Perform ETL tasks, enhancements, validation, and maintenance of the programs and templates on an ongoing basis.
  • Perform QC, lead unit testing activities, develop validation scripts for user acceptance, manage and execute programs and dry runs as needed, and resolve programming issues proactively.
  • Develop and maintain mapping, and program specifications for standard reports, listings, and visualizations.
  • Maintain database programming checklists and trackers to ensure conformance of high-quality deliverables with the study data validation and reporting package.
  • Establish and implement programming standards and comply with regulatory requirements among project team members and across all studies.
  • Participate in the development of and ensure compliance to Standard Operating Procedures (SOPs), policies, and guidelines.

Experience:
  • Minimum of 5 years database programming experience and data validation programming in the device/pharmaceutical/CRO industry.
  • Expertise in Clinical Programming, methods, and techniques
  • Expertise in using standard reporting and data visualization tools including JReview, and SAS tools.
  • Knowledge of industry standard clinical technologies including CTMS, EDC (RAVE, InForm)
  • Knowledge of CDISC data standards.
  • Knowledge and understanding of relational databases.
  • Clinical Programming, Project Management, and Technical Expertise
  • Knowledge of logical data design and data mapping
  • Knowledge of reporting and data visualization tools: JReview, Spotfire, SAS suite and ETL technology
  • Experience with programming development, validation, execution, maintenance, documentation, and archival of clinical data for regulatory submission is required.
  • Proficient in industry standards, medical terminology, and clinical trial methodologies.

Education:
  • Bachelor of Science degree in Computer Science, Mathematics, or related area with relevant experience
  • Other degrees and certifications considered if commensurate with related data management experience

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