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Clinical Trials Data Analyst Jobs (NOW HIRING)

Systimmune

Clinical Data Analyst, Spotfire

Redmond, WA · On-site

$90K - $130K/yr

Alongside ongoing clinical trials. SystImmune has a robust preclinical pipeline of potential cancer ... The Spotfire Clinical Data Analyst will specialize in the installation, maintenance, and ...

CG Oncology, Inc.

Senior Clinical Trials Scientist

$150K - $170K/yr

About the role The Senior Clinical Trials Scientist (Sr CTS) provides scientific leadership and ... data analysis, and reporting. The ideal candidate is a seasoned professional with demonstrated ...

Prolaio

Data Architect, Clinical

Chicago, IL · On-site

$65.75 - $84.50/hr

... analytics, data science, clinical operations, quality, and other enterprise use cases in a ... Design and govern conceptual, logical, and physical data models for clinical trials, cardiovascular ...

Prolaio

Data Architect, Clinical

Chicago, IL

$65.75 - $84.50/hr

... analytics, data science, clinical operations, quality, and other enterprise use cases in a ... Design and govern conceptual, logical, and physical data models for clinical trials, cardiovascular ...

Tango Therapeutics

Clinical Trials Manager

Boston, MA · On-site

Monitor CRO/ vendor performance and ensure timely and accurate data integration, transfer, and ... Strong analytical thinking and decision-making capabilities * Willingness to travel, as required ...

GDIT

Clinical Research Data Analyst

Fort Liberty, NC · Hybrid

$57K - $60K/yr

The Research Data Analyst will coordinate activities associated with clinical trials in the area of Traumatic Brain Injury (TBI) and provides assurance of accurate documentation in compliance with ...

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Clinical Trials Data Analyst information

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How much do clinical trials data analyst jobs pay per hour?

As of Jun 12, 2026, the average hourly pay for clinical trials 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 the key skills and qualifications needed to thrive in the Clinical Trials Data Analyst position, and why are they important?

To thrive as a Clinical Trials Data Analyst, you need strong analytical abilities, a solid understanding of biostatistics, knowledge of clinical trial processes, and a relevant degree in life sciences, statistics, or a related field. Familiarity with statistical programming languages like SAS or R, experience using clinical data management systems (such as Medidata or Oracle Clinical), and certifications like SAS Certified Clinical Trials Programmer are highly valuable. Excellent attention to detail, problem-solving skills, and the ability to collaborate effectively with cross-functional teams are important soft skills. These qualifications ensure accurate data analysis, regulatory compliance, and effective communication of findings, all vital to advancing clinical research outcomes.

How much do clinical data analysts make?

Clinical trials data analysts typically earn a median salary ranging from $60,000 to $85,000 annually, depending on experience, education, and location. Entry-level positions may start around $50,000, while experienced analysts with specialized skills can earn over $100,000. Certifications in data analysis tools like SAS or SQL can enhance earning potential.

What is a Clinical Trials Data Analyst job?

A Clinical Trials Data Analyst is responsible for collecting, processing, and analyzing data from clinical studies to ensure accuracy, compliance, and statistical validity. They work with clinical researchers, data managers, and regulatory teams to interpret trends, validate findings, and report results. Their role is crucial for ensuring that clinical trial data meets regulatory standards and provides meaningful insights for drug development or medical research. Strong skills in statistical analysis, database management, and regulatory compliance are essential for this role.

What are the typical daily tasks and team interactions for a Clinical Trials Data Analyst?

As a Clinical Trials Data Analyst, your daily responsibilities often include cleaning and validating clinical data, performing statistical analyses, and generating reports or visualizations for study teams. You will closely collaborate with clinical researchers, data managers, statisticians, and project managers to ensure data integrity and address study objectives. Regular participation in team meetings, updates with cross-functional departments, and presenting analysis results are also common parts of the role. This teamwork is essential for successfully running clinical trials and delivering reliable insights to support regulatory submissions and medical advancements.

Will AI replace data analyst?

AI is transforming the role of Clinical Trials Data Analysts by automating routine data processing and analysis tasks, but it is unlikely to fully replace the need for human expertise in interpreting complex clinical data, ensuring data quality, and making strategic decisions. Analysts will increasingly work alongside AI tools, requiring skills in data management, statistical analysis, and familiarity with AI applications. Human judgment remains essential for contextual understanding and ethical considerations in clinical research.

What does a clinical trial analyst do?

A clinical trial analyst is responsible for collecting, managing, and analyzing data from clinical studies to ensure accuracy and compliance with regulatory standards. They use statistical tools and software to interpret trial results, prepare reports, and support decision-making in the drug development process. Strong attention to detail and knowledge of Good Clinical Practice (GCP) are essential for this role.

Can a data analyst become a clinical analyst?

A clinical trials data analyst can transition to a clinical analyst role by gaining broader knowledge of clinical operations, regulatory requirements, and healthcare systems. Developing skills in project management, clinical software, and certifications like RAC or CCR can facilitate this career progression.
More about Clinical Trials Data Analyst jobs
What cities are hiring for Clinical Trials Data Analyst jobs? Cities with the most Clinical Trials Data Analyst job openings:
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Clinical Trials Data Analyst jobs near you
Infographic showing various Clinical Trials Data Analyst job openings in the United States as of June 2026, with employment types broken down into 3% Locum Tenens, 4% As Needed, 14% Full Time, 73% Part Time, 3% Temporary, and 3% Contract. Highlights an 81% Physical, 8% Hybrid, and 11% Remote job distribution, with an average salary of $75,625 per year, or $36.4 per hour.
Clinical Data Analyst, Spotfire

Clinical Data Analyst, Spotfire

Systimmune

Redmond, WA • On-site

$90K - $130K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 10 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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