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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.
Key Qualifications:
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.
Required Skills, Experience, and Education:
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.
