Clinical Data Visualization Programmer

Redmond, WA
Full Time
Clinical Development
Mid Level

Summary: This job requires recent working experience with data visualization tools for clinical data visualizations, creating dashboards for real time data review, metrics, and surveillance. Also, this job requires SAS/R programming skills and industry experience working with clinical trial data.

SystImmune Inc. is a clinical-stage biopharmaceutical company located in Redmond, WA. It specializes in developing innovative cancer treatments using its established drug development platforms, focusing on bi-specific, multi-specific antibodies, and antibody-drug conjugates (ADCs). SystImmune has several assets in various stages of clinical trials for solid tumor and hematologic indications. Alongside ongoing clinical trials, SystImmune has a strong preclinical pipeline of potential cancer therapeutics in the discovery or IND-enabling stages, representing cutting-edge biologics development. 

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.

Job Responsibilities: 

  • This role will create, lead, and drive activities to assess and develop the Analytics and Reporting functions.
  • Programs metrics and reports in data visualization tool/analyst software (e.g., JReview, Power BI, Spotfire).
  • DevelopSAS Protocol Deviation listings, Patient Profiles, and other ad-hoc data listings for internal review.
  • Ability to independently develop innovative and complex reports to support activities including, but not limited to, data review, surveillance, and reconciliation.
  • Develops and maintains the Analytics and Reporting Global Library to ensure consistency across programs and studies and concordance with the EDC Global Library.
  • Trains Clinical Data Managers on how to generate output (e.g., data review tool, metrics).
  • Fosters effective cross-functional communication with study teams and other internal and external stakeholders to develop new or improve existing data review tools.
  • Coordinates 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.
  • May contribute to the development, review and implementation of SOPs, templates and processes and other departmental and/or cross functional initiatives.
  • Utilizes experience and leadership skills to provide guidance to other team members.
  • Takes ownership of process resources available to team.
  • Implements SystImmune strategies, initiatives, processes, and standards to support timelines and deliverables for quality data.
  • Aligns with protocol, ICH GCP, and regulatory requirements.
  • Provides and maintains documentation to support activities.

Qualifications:

  • 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).


The hiring pay range for this position is $110,000 - $170,000 per year based on skills, education, and experience relevant to the role.

SystImmune is a leading and well-funded clinical-stage biopharmaceutical company located in Redmond, WA and Princeton, NJ. It specializes in developing innovative cancer treatments using its established drug development platforms, focusing on bi-specific, multi-specific antibodies, and antibody-drug conjugates (ADCs). SystImmune has multiple assets in various stages of clinical trials for solid tumor and hematologic indications. Alongside ongoing clinical trials, SystImmune has a robust preclinical pipeline of potential cancer therapeutics in the discovery or IND-enabling stages, representing cutting-edge biologics development. We offer an opportunity for you to learn and grow while making significant contributions to the company’s success. SystImmune offers a comprehensive benefits package. 

SystImmune is an Equal Opportunity Employer. We welcome diverse talent and encourage all qualified applicants to apply.

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