Senior Statistical Programmer with TABLEAU (Contract, Remote) at Elan Solutions in NY, United States

Job description

• Location: Remote (home-based in the U.S.)
• Work Time Zone: Eastern Time Zone (EST)
• Employment Type: 12-month contract (renewable)
• Please NOTE: This role requires over 8 years of hands-on SAS programming experience and expertise in Tableau within the pharmaceutical and biotech industry.

Responsibilities

• Create, manage, and optimize dashboards, reports, and visualizations in clinical trial data contexts.
• Provide programming support for generating tables, listings, and figures for assigned projects.
• Set up studies and generate visualizations using Tableau, preprocess clinical data using SAS, assess quality of analysis data, and perform cross-study analyses.
• Create and validate safety tables, efficacy tables, and lab shift tables in line with SAP and mock layouts, and validate datasets and outputs through double programming.
• Participate in process improvement initiatives, internal programming tasks, and presentations to internal committees and boards.

Requirements

• - Tableau Expertise: At least 4+ years of experience in creating, managing, and optimizing dashboards, reports, and visualizations in clinical trial data contexts.
• - SAS Programming: Over 8 years of industry experience working with clinical trial data as a SAS/Statistical Programmer.
• - Oncology Experience: 4-5 years of experience in oncology-focused clinical trials and overseeing CRO activities.
• - Data Visualization: Recent experience in producing data visualizations using Tableau, such as real-time data review dashboards.
• - Study Setup and Analysis: Experience in setting up studies and generating visualizations using Tableau, preprocessing clinical data using SAS, assessing the quality of analysis data, and performing cross-study analyses.
• - Collaboration: Strong collaboration skills with staff in Biostatistics, Clinical Data Management, Clinical Research, and Global Drug Safety.
• - Programming Support: Ability to provide programming support for generating tables, listings, and figures for assigned projects.
• - CDISC Standards: Knowledge and application of CDISC standards (SDTM, ADaM) to submission activities.
• - Validation: Experience in creating and validating safety tables, efficacy tables, and lab shift tables in line with SAP and mock layouts and validating datasets and outputs through double programming.
• - Process Improvement: Participation in process improvement initiatives, internal programming tasks, and presentations to internal committees and boards.
• - A master’s or bachelor’s degree (or equivalent qualification) in a relevant field or 10 years of industry experience.
• - 4+ years of expertise in Tableau (mandatory).
• - 8+ years of experience in statistical programming with clinical trial data, particularly using SAS software.
• - Strong communication and collaboration skills, with a proven ability to thrive in a multidisciplinary team environment.
• - Prior experience in oncology-focused clinical trials is preferred.
• - Exceptional time management and organizational abilities to meet deadlines and deliver high-quality results.
• Tableau

Skills

Required

• Tableau
• SAS programming
• Statistical programming
• Data visualization
• CDISC standards (SDTM, ADaM)
• Double programming
• Validation of datasets and outputs
• Collaboration
• Communication
• Time management
• Organizational abilities

Preferred

• Oncology experience