Job Description
Job DescriptionW2 Role:
Spotfire Developer – Life Sciences / Pharmaceutical
Location: Trenton, New Jersey – Onsite
Industry: Pharmaceutical / Life Sciences
Experience: Overall IT experience 10+
We are seeking an experienced Spotfire Developer to support one of our pharmaceutical clients in New Jersey. The ideal candidate will have strong hands-on experience developing TIBCO Spotfire dashboards and analytical applications using clinical, safety, PK/PD, and real-world evidence data.
???? Key Responsibilities:
• Design, develop, and maintain TIBCO Spotfire dashboards and analytical applications
• Connect Spotfire with SQL, SAS, cloud data sources, and healthcare data platforms
• Work with clinical data structured around CDISC SDTM/ADaM standards
• Develop IronPython/Python scripts and custom Spotfire expressions
• Build PK/PD visualizations including exposure-response, concentration-time, and dose-response analyses
• Develop pharmacovigilance (PV) and safety dashboards for AE/SAE review, signal detection, and safety monitoring
• Partner with biostatisticians, clinical programmers, data managers, clinical pharmacology, and drug safety teams
• Optimize Spotfire dashboards for large clinical and longitudinal datasets
• Troubleshoot data connectivity, refresh, and dashboard performance issues
• Support validation, documentation, and change-control activities in a GxP-regulated environment
???? Required Skills:
✅ 5+ years of hands-on TIBCO Spotfire development
✅ Strong SQL skills
✅ Hands-on IronPython/Python scripting within Spotfire
✅ Experience with clinical, healthcare, or RWE data
✅ Knowledge of CDISC SDTM/ADaM
✅ Experience with PK/PD analytics and visualization
✅ Experience with pharmacovigilance / safety analytics
✅ AE/SAE review and safety monitoring experience
✅ Strong stakeholder/client-facing communication skills
✅ Bachelor's degree in Life Sciences, Computer Science, Statistics, or related field
???? Preferred:
• Spotfire Consultant-level certification
• 21 CFR Part 11 / validated systems experience
• R, Snowflake, or AWS experience
• Pharmaceutical or CRO client-site experience
• NCA / population PK/PD exposure
• MedDRA / WHO-DD knowledge
• DSUR/PBRER and standard safety outputs experience