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Clinical Trials Data Analyst Jobs (NOW HIRING)

This full-time remote position entails ensuring data integrity for various research studies ... Working knowledge of clinical trials, Federal, State, and Local Regulations, and IRB requirements.

This full-time remote position entails ensuring data integrity for various research studies ... Working knowledge of clinical trials, Federal, State, and Local Regulations, and IRB requirements.

A Clinical Data Analyst (or Clinical Informatics Analyst) is a clinical research information professional responsible for verifying the validity of clinical trials and data gathered. He/she will ...

A Clinical Data Analyst (or Clinical Informatics Analyst) is a clinical research information professional responsible for verifying the validity of clinical trials and data gathered. He/she will ...

... a Clinical Trials Coverage Analyst in a fully remote capacity, supporting a leading academic ... Proficiency in document and data management tools, including Microsoft Word, Excel, PowerPoint ...

Protocol Data Analyst I Department: Research Employment Type: Full Time Location: National Institue ... This role codes clinical trials using the NCI Thesaurus, abstracts biomarkers, processes accrual ...

Position: Clinical Data Analyst Location: - Remote(CST working hours) Experience: -10+ Years ... Prioritize clinical trials and assess opportunities for content expansion (e.g., biomarkers, prior ...

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 ...

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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 Jul 13, 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.

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.

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:
What are the most commonly searched types of Clinical Trials Data Analyst jobs? The most popular types of Clinical Trials Data Analyst jobs are:
What states have the most Clinical Trials Data Analyst jobs? States with the most job openings for Clinical Trials Data Analyst jobs include:
Infographic showing various Clinical Trials Data Analyst job openings in the United States as of July 2026, with employment types broken down into 1% Locum Tenens, 1% Internship, 86% Full Time, 6% Part Time, 1% Temporary, and 5% Contract. Highlights an 82% Physical, 5% Hybrid, and 13% Remote job distribution, with an average salary of $75,625 per year, or $36.4 per hour.
Clinical Trials Data Assistant

Clinical Trials Data Assistant

Northwestern University

Evanston, IL • On-site

$11/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 12 days ago


Northwestern University rating

7.8

Company rating: 7.8 out of 10

Based on 47 frontline employees who took The Breakroom Quiz

179th of 553 rated colleges and universities


Job description

Department: MED-Cancer Center
Salary/Grade: NEX/11
Target hiring range for this position will be between be range is as be $23.71-$28.00 per hour . Offered salary will be determined by the applicant's education, experience, knowledge, skills and abilities, as well as internal equity and alignment with market data.
Job Summary:
Ensures submission and maintenance of accurate, timely, complete and reliable data and reports by implementing data management and quality assurance procedures. Provides feedback to customers and clients regarding systematic data errors or problems. Documents revisions in codebooks and manuals.
  • Responsible for the compilation of all data for clinical trials managed by the CTO. Manages project data including extraction, entering, processing, accuracy, analysis and evaluation of data ensuring that results meet project information and deliverable objectives.
  • Serves as a resource to new staff regarding quality data entry, maintenance, and departmental policies. Assists with data for all teams and occasional audits. Partners with internal/external project and IT staff to create, review, analyze, interpret, summarize and prepare progress and final reports.
  • Provides consultation to internal/external project staff on appropriate data management, methodological issues and analysis of data
Specific Responsibilities:
Strategic Planning
  • Participates in team and other departmental meetings to share experiences, learn about what other teams are doing and help solve problems.
Administration
  • Manages data receipt, tracking and follows up on assigned project(s).
  • Detects trends and reports on patterns of errors.
  • Contacts customers to obtain missing data.
  • Compiles and maintains codebooks, data files and memos needed for subsequent analysis of data.
  • Learns and complies with appropriate compliance and regulation requirements regarding protected data.
  • Obtains required training for all electronic data capture systems.
  • Gives input on CTO policies and procedures with regards to data entry/monitoring.
  • Assesses protocol compliance and communicates directly with the study coordinator and PI when compliance issues are identified.
Development
  • Edits, codes and enters data per protocol.
  • Runs reports and completes basic analysis.
  • Determines data needed to be collected and the appropriate data resources for specific study/project needs.
  • Abstract all required patient data from medical record sources for entry into cas report forms (paper and/or electronic).
  • Main contact for monitors/CRO's for data query resolution.
Performance
  • Reviews data input for accuracy, addressing on skip patterns, coding, and other information.
  • Performs cleaning/formatting tasks of datasets.
  • Follow timelines stated in SOP (CO-SM-312) and individual sponsor contracts, for data entry and query resolution.
  • Assists with data reconciliation
Miscellaneous
Performs other duties as assigned.
Minimum Qualifications:
  • A high school diploma or equivalent is required.
  • 2 years' data entry or similar experience is required.
  • Please see information highlighted below.
  • Enterprise Applications
  • eIRB
  • Kronos
  • Infrastructure
  • Mac OS X Operating System
  • Microsoft Exchange
Minimum Competencies: (Skills, knowledge, and abilities.)
  • Ability to understand complex pathology data and cancer treatment regimens and their toxicity.
  • Ability to establish and maintain effective working relationships with patients, physicians, nurses, technicians and coworkers.
  • Excellent verbal and written communication
  • Medical terminology
Preferred Qualifications:
  • Successful completion of a full 4-year course of study in an accredited college or university leading to a bachelor's or higher degree; OR appropriate combination of education and experience.
  • Experience in data management in a health field, exposure to cancer clinical trials.
  • Computer literate in basic software, internet use, and cancer-related databases.
Preferred Competencies: (Skills, knowledge, and abilities)
  • Experience with oncology clinical trials
  • Experience with databases such as SAS/Access
Benefits:
At Northwestern, we are proud to provide meaningful and competitive benefits. The available benefits package for this position will include health, dental, vision, disability, and life insurance; paid vacation and holidays; paid medical/sick and parental leave; tuition benefits for the employee and dependents; pre-tax and flex spending accounts for commuting and dependent care; generous retirement savings options; and wellness programs. For a comprehensive overview of available benefits, including eligibility details, visit us at https://www.northwestern.edu/hr/benefits/index.html to learn more.
Work-Life and Wellness:
Northwestern offers comprehensive programs and services to help you and your family navigate life's challenges and opportunities, and adopt and maintain healthy lifestyles.
We support flexible work arrangements where possible and programs to help you locate and pay for quality, affordable childcare and senior/adult care. Visit us at https://www.northwestern.edu/hr/benefits/work-life/index.html to learn more.
Professional Growth & Development:
Northwestern supports employee career development in all circumstances whether your workspace is on campus or at home. If you're interested in developing your professional potential or continuing your formal education, we offer a variety of tools and resources. Visit us at https://www.northwestern.edu/hr/learning/index.html to learn more
Northwestern University is an Equal Opportunity Employer and does not discriminate on the basis of protected characteristics, including disability and veteran status. View Northwestern's non-discrimination statement . Job applicants who wish to request an accommodation in the application or hiring process should contact the Office of Civil Rights and Title IX Compliance. View additional information on the accommodations process .

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