Spotfire Developer role at Trenton NJ

Job Description

Job Description

W2 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