Clinical Data Visualization Programmer

$110,000 - $170,000/Yr

SystImmune - Redmond, WA

Full-time - Mid Level

Redmond, WA

Chemical Manufacturing

About the position

The Clinical Data Visualization Programmer (CDVP) works collaboratively with Data Management, Biostatistics, Statistical Programming, Clinical Science, and Clinical Operations to ensure the high-quality production of visualizations for data review, surveillance, and reconciliation using JReview, Spotfire, Power BI, and other visualization tools. Additionally, the CDVP will develop and maintain SAS/R data listings for use by the internal SystImmune team.

Responsibilities

• Create, lead, and drive activities to assess and develop the Analytics and Reporting functions.
• Program metrics and reports in data visualization tool/analyst software (e.g., JReview, Power BI, Spotfire).
• Develop SAS Protocol Deviation listings, Patient Profiles, and other ad-hoc data listings for internal review.
• Independently develop innovative and complex reports to support activities including, but not limited to, data review, surveillance, and reconciliation.
• Develop and maintain the Analytics and Reporting Global Library to ensure consistency across programs and studies and concordance with the EDC Global Library.
• Train Clinical Data Managers on how to generate output (e.g., data review tool, metrics).
• Foster effective cross-functional communication with study teams and other internal and external stakeholders to develop new or improve existing data review tools.
• Coordinate with Clinical Data Managers regarding timelines and deliverables to ensure all reports are working as expected.
• Independently manage processes and applications while evaluating for improvements; lead working groups to develop and implement new processes and applications.
• Contribute to the development, review and implementation of SOPs, templates and processes and other departmental and/or cross functional initiatives.
• Utilize experience and leadership skills to provide guidance to other team members.
• Take ownership of process resources available to team.
• Implement SystImmune strategies, initiatives, processes, and standards to support timelines and deliverables for quality data.
• Align with protocol, ICH GCP, and regulatory requirements.
• Provide and maintain documentation to support activities.

Requirements

• Minimum of 5 years of experience with Analyst software (e.g., Spotfire, Power BI, Tableau), preferably in the pharmaceutical or biotechnology industry.
• Bachelor's degree in biostatistics, computer science, biology, pharmacology or related.
• Technical expertise in database and report development.
• Experience with programming languages (e.g., SQL, Python).
• Strong proficiency in SAS and R, including data step programming, PROC SQL, and R packages for data analysis.
• Experience with CDISC standards (SDTM, ADaM).
• Experience in managing projects as well as effective verbal and written communication skills.
• Ability to work independently, organize tasks, time and priorities, ability to multi-task.
• Knowledge of and experience with clinical databases, electronic data capture systems, quality control processes and auditing procedures.
• Strong critical thinking skills.
• Familiarity with GCP, ICH and FDA requirements as they apply to clinical data.
• Strong well-rounded technical skills (EDC systems, MS Word, Excel, PowerPoint).

Benefits

• 100% paid employee premiums for medical/dental/vision
• STD, LTD
• 401(k) plan with a 50% company match of up to 3% and a vesting schedule of only 5 years
• 15 PTO days per year
• Sick leave
• 11 paid holidays