Clinical Data Visualization Programmer
Redmond, WA
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 stable, well-funded biotech company with a bright future. 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 including: 100% paid employee premiums for medical/dental/vision, also STD, LTD, a 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, plus 11 paid holidays and MORE.
SystImmune is an Equal Opportunity Employer. Interested applicants should send their CV and cover letter to [email protected]
