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Full Time Clinical Data Analyst Jobs (NOW HIRING)

Systimmune

Clinical Data Analyst, Spotfire

Redmond, WA · On-site

$90K - $130K/yr

This position requires a full-time onsite presence at our Redmond, WA office. Responsibilities: * Lead the installation, configuration, and ongoing maintenance of Spotfire for clinical data analysis ...

SystImmune, Inc

Clinical Data Analyst, Spotfire

Redmond, WA · On-site

$90K - $130K/yr

This position requires a full-time onsite presence at our Redmond, WA office. Responsibilities: * Lead the installation, configuration, and ongoing maintenance of Spotfire for clinical data analysis ...

Jj

Clinical Database Programmer-EDC

Raynham, MA

Data Analytics & Computational Sciences Job Sub Function: Clinical Data Management Job Category: Professional All Job Posting Locations: Raynham, Massachusetts, United States of America, Warsaw ...

Jj

Clinical Database Programmer-EDC

Warsaw, IN

Data Analytics & Computational Sciences Job Sub Function: Clinical Data Management Job Category: Professional All Job Posting Locations: Raynham, Massachusetts, United States of America, Warsaw ...

Clover Health

Senior Clinical Data Analyst

As a Senior Clinical Data Analyst in the Clover Care Services (CCS) organization, you will help drive better patient outcomes, improve care coordination, and optimize resource utilization by ...

Newfire Global Partners

Clinical Analyst

Boston, MA · Remote

$110K - $156K/yr

Clinical Data Analyst Department: Product Location: Care Lumen | Remote (US Only) Employment Type: Full-time Employee Salary Range: $110,000 - $156,000 Scope The Clinical Data Analyst is a hands-on ...

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How much do full time clinical data analyst jobs pay per hour?

As of Jun 10, 2026, the average hourly pay for full time clinical data analyst in the United States is $36.36, according to ZipRecruiter salary data. Most workers in this role earn between $29.33 and $42.07 per hour, depending on experience, location, and employer.

What are some common challenges faced by Full Time Clinical Data Analysts, and how can they be addressed?

Full Time Clinical Data Analysts often encounter challenges such as ensuring data accuracy, managing large and complex datasets, and staying updated with evolving regulatory requirements. Collaboration with clinical teams and IT departments is crucial for resolving data discrepancies and maintaining data integrity. Regular training on new data management tools and compliance standards, as well as effective communication with cross-functional teams, helps analysts overcome these challenges and contribute to successful clinical research outcomes.

What are the key skills and qualifications needed to thrive as a Full Time Clinical Data Analyst, and why are they important?

To thrive as a Full Time Clinical Data Analyst, you need strong analytical skills, knowledge of clinical research methodologies, and a degree in a related field such as health informatics, statistics, or life sciences. Expertise in statistical software (e.g., SAS, R), databases (SQL), and familiarity with electronic health record (EHR) systems or data management certifications are typically required. Attention to detail, problem-solving abilities, and effective communication are crucial soft skills for collaborating with clinical teams and translating data insights. These skills ensure accurate data analysis, support evidence-based decision-making, and drive improvements in patient outcomes and research quality.

What does a Full Time Clinical Data Analyst do?

A Full Time Clinical Data Analyst is responsible for collecting, managing, and analyzing clinical data to support healthcare research, improve patient care, and ensure regulatory compliance. They work with large datasets from clinical trials, electronic health records, and other sources to identify trends, generate reports, and assist in decision-making processes. Their role often involves using statistical software, maintaining data integrity, and collaborating with other healthcare professionals to provide meaningful insights from complex clinical information.
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Full Time Clinical Data Analyst jobs near you
Clinical Data Analyst, Spotfire

Clinical Data Analyst, Spotfire

Systimmune

Redmond, WA • On-site

$90K - $130K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 9 days ago

Job description

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 discover and 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.
The Spotfire Clinical Data Analyst will specialize in the installation, maintenance, and development of clinical data visualizations utilizing Spotfire. This role emphasizes creating and enhancing Spotfire-based patient profiles, real-time data review dashboards, clinical metrics dashboards, and other customized visualization reports such as live TLFs. Additionally, the Analyst will collaborate closely with Clinical Data Management, Biostatistics, Clinical Science, and Clinical Operations to optimize data visualization strategies.
This position requires a full-time onsite presence at our Redmond, WA office.
Responsibilities:
  • Lead the installation, configuration, and ongoing maintenance of Spotfire for clinical data analysis and visualization.
  • Design, develop, and maintain Spotfire dashboards for patient profiles, real-time clinical data review, surveillance, metrics tracking, and other customized visualizations.
  • Develop sophisticated, interactive visualizations to support internal data review processes, surveillance, reconciliation, and reporting needs.
  • Collaborate with Clinical Data Managers, Biostatistics, Clinical Operations, and Clinical Science teams to identify requirements and translate them into effective Spotfire visualizations.
  • Manage and continually improve the Spotfire analytics environment, ensuring data integrity, accuracy, and performance.
  • Establish and maintain a Global Spotfire Library, aligning visualization standards across multiple studies and programs.
  • Train and mentor Clinical Data Managers and other stakeholders in effectively utilizing Spotfire dashboards and reports.
  • Coordinate timelines and deliverables with Clinical Data Management and other cross-functional teams to ensure visualizations meet expectations.
  • Contribute to the evaluation and implementation of new technologies and methodologies to enhance Spotfire capabilities.
  • Document visualization specifications, maintain clear documentation for Spotfire-related processes, and contribute to departmental SOPs.
  • Uphold industry standards including protocol compliance, ICH GCP, FDA regulations, and CDISC standards (SDTM, ADaM).

Qualifications:
  • Bachelor’s degree in Biostatistics, Computer Science, Life Science, or a related field.
  • Minimum of 5 years of hands-on experience in Spotfire visualization development and administration in a clinical trial setting, preferably in oncology and hematology.
  • Expert-level proficiency in Spotfire including installation, configuration, dashboard development, data integration, scripting (IronPython, TERR, etc.) and performance optimization.
  • Strong experience developing patient profiles, real-time data review dashboards, clinical metrics dashboards, and complex reports.
  • Experience with SAS/R, SQL programming, and data manipulation.
  • Familiarity with clinical trial data standards (CDISC SDTM, ADaM), experience with TLF generation preferred.
  • Experience integrating Spotfire with clinical databases and EDC systems (e.g., Medidata RAVE, Oracle Inform, Veeva).
  • Strong organizational skills, critical thinking, and the ability to manage multiple projects simultaneously.
  • Excellent verbal and written communication skills.
  • Familiarity with regulatory guidelines including GCP, ICH, and FDA requirements.
  • Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).

Compensation and Benefits:
The expected base salary range for this position is $90,000 - $130,000 annually. Actual compensation will be based on a variety of factors, including but not limited to a candidate’s qualifications, experience, and skills.
SystImmune is a leading and 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.
We offer an opportunity for you to learn and grow while making significant contributions to the company’s success.
SystImmune is an Equal Opportunity Employer. We welcome diverse talent and encourage all qualified applicants to apply.

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