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Clinical Data Associate Jobs in Kansas (NOW HIRING)

Associate Data Engineer

Kansas City, KS

$110K - $132K/yr

Description of the Role As an Associate Data Engineer at Vytalize Health, you will support the data ... clinical data infrastructure. You will learn to think about data quality metrics, testing, and ...

CRA II and Senior CRA

Lawrence, KS · Remote

$91K - $114K/yr

We are currently seeking a Clinical Research Associate (Level II or Senior) to join our diverse and ... Performing data review and resolution of queries to maintain high-quality clinical data.

IQVIA is hiring Senior Clinical Research Associate 1 with experience in either oncology ... data as required by the study protocol, applicable regulations and guidelines, and sponsor ...

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Clinical Data Associate information

See Kansas salary details

$12

$34

$77

How much do clinical data associate jobs pay per hour?

As of Jul 31, 2026, the average hourly pay for clinical data associate in Kansas is $34.74, according to ZipRecruiter salary data. Most workers in this role earn between $26.15 and $34.71 per hour, depending on experience, location, and employer.

What are some common challenges faced by Clinical Data Associates when ensuring data quality during clinical trials?

Clinical Data Associates often encounter challenges such as identifying and resolving discrepancies in large datasets, maintaining strict compliance with regulatory standards, and coordinating timely data entry from multiple sites. They must work closely with clinical research teams and data managers to clarify ambiguous data and implement data cleaning procedures. Staying organized and detail-oriented is essential to ensure data accuracy and the successful progression of clinical trials.

Which is better, CDM or SAS?

For a Clinical Data Associate, SAS is a widely used software for data analysis and reporting in clinical trials, while CDM (Clinical Data Management) refers to the overall process of collecting, cleaning, and managing clinical data, often using various tools including SAS. SAS skills are highly valued in the role, but understanding the broader CDM process is also important for effective data handling and compliance.

What's next after CRC?

After working as a Clinical Research Coordinator (CRC), professionals often advance to roles such as Clinical Data Associate, Clinical Trial Manager, or Regulatory Affairs Specialist. Gaining experience, certifications like CCRP, and developing skills in data management and regulatory compliance can facilitate career progression in clinical research.

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

To thrive as a Clinical Data Associate, you need a solid understanding of clinical research, data management principles, and attention to detail, often supported by a degree in life sciences or a related field. Familiarity with clinical data management systems (CDMS), electronic data capture (EDC) tools, and knowledge of regulatory guidelines like GCP or CDISC is typically required. Strong organizational skills, analytical thinking, and clear communication set outstanding candidates apart in this role. These skills ensure the accuracy, integrity, and compliance of clinical trial data, which are crucial for successful research outcomes and regulatory approval.

What does a Clinical Data Associate do?

A Clinical Data Associate is responsible for collecting, validating, and managing clinical trial data to ensure its accuracy, completeness, and compliance with regulatory standards. They work closely with clinical research teams to monitor data quality, resolve discrepancies, and prepare data for analysis. Their work is essential in supporting drug development and regulatory submissions by ensuring reliable and high-quality clinical data.

What is the role of a clinical data associate?

A clinical data associate is responsible for collecting, managing, and ensuring the accuracy of data from clinical trials. They review data for completeness, resolve discrepancies, and use database tools to support data integrity and regulatory compliance throughout the trial process.

What Does a Clinical Data Associate Do?

A clinical data associate is responsible for tracking data and results in a research study. As a clinical data associate, your job duties are to collect data, perform data management, and input data into any software used by your team. You work on a research team, so you must be able to work collaboratively and have excellent organizational skills. While you spend most of your time in an office, you may be required to work in the field to record data. The only universal qualifications needed for this career are a background in health care or medical science research and experience with data management software like Oracle Clinical, Microsoft Excel, and SPSS.

Do you need a degree to be a CRC?

A Clinical Data Associate (CDA) typically does not require a specific degree, but a background in life sciences, healthcare, or related fields is often preferred. Many employers value relevant certifications and experience with clinical data management tools. Educational requirements can vary by employer and job level.

Is CRA an entry level job?

A Clinical Data Associate (CDA) role is typically considered an entry-level position in clinical research, often requiring a bachelor's degree in a related field and some familiarity with data management tools. However, a Clinical Research Associate (CRA) role usually requires more experience and is considered a mid- to senior-level position, involving site monitoring and regulatory compliance. Entry-level roles may serve as a stepping stone toward CRA positions with additional experience and certifications.

What is the difference between Clinical Data Associate vs Clinical Research Coordinator?

AspectClinical Data AssociateClinical Research Coordinator
Primary RoleManage and ensure accuracy of clinical trial dataOversee trial operations, patient recruitment, and site management
CredentialsBachelor's in life sciences or related field; familiarity with data managementBachelor's in health sciences or related field; clinical trial experience
Work EnvironmentData management teams, clinical trial databasesClinical sites, hospitals, research facilities
Industry UsagePharmaceutical companies, CROs, biotech firmsHospitals, research institutions, clinical trial sites

While both roles support clinical trials, a Clinical Data Associate primarily focuses on managing and validating trial data, ensuring accuracy and compliance. In contrast, a Clinical Research Coordinator handles the overall trial operations, including patient recruitment and site coordination. Both roles require relevant certifications and work within the clinical research industry, but their daily responsibilities differ significantly.

What are the most commonly searched types of Clinical Data jobs in Kansas? The most popular types of Clinical Data jobs in Kansas are:
What are popular job titles related to Clinical Data Associate jobs in Kansas? For Clinical Data Associate jobs in Kansas, the most frequently searched job titles are:
What job categories do people searching Clinical Data Associate jobs in Kansas look for? The top searched job categories for Clinical Data Associate jobs in Kansas are:
Infographic showing various Clinical Data Associate job openings in Kansas as of July 2026, with employment types broken down into 71% Full Time, and 29% Contract. Highlights an 100% In-person job distribution, with an average salary of $72,258 per year, or $34.7 per hour.

Associate Data Engineer

Vytalize Health

Kansas City, KS

$110K - $132K/yr

Full-time

Posted 17 days ago


Job description

Description of the Role

As an Associate Data Engineer at Vytalize Health, you will support the data engineering team by handling critical operational tasks, resolving support tickets, and conducting discovery work that enables our senior engineers to stay focused on building and scaling data platforms. You will work with healthcare data pipelines, learn production data systems, and contribute to improving data quality, reliability, and documentation.
This is an ideal role for someone early in their data engineering career or transitioning into data engineering from a related field. You will be mentored by experienced data engineers, gain hands-on experience with real healthcare data, and learn both classical data engineering practices and modern platforms like Databricks. Your contributions—from fixing bugs to documenting systems to investigating data quality issues—directly support the reliability of our clinical data infrastructure. You will learn to think about data quality metrics, testing, and validation as core responsibilities.

Primary Responsibilities

  • Handle support tickets and operational issues reported by internal teams and external partners; investigate root causes and coordinate resolution with senior engineers

  • Perform KTLO (Keep The Lights On) tasks including monitoring pipeline health, responding to alerts, validating data quality, and investigating data anomalies

  • Conduct data source discovery and profiling work — examining raw data sources, documenting data structure, identifying quality issues, and recommending integration approaches

  • Assist with data validation and testing — writing SQL queries to validate data transformations, identifying gaps and inconsistencies, and flagging issues for review

  • Support data quality initiatives by running diagnostics, documenting data quality findings, and escalating issues with clear context for senior engineers

  • Assist in establishing and monitoring data quality metrics — working with senior engineers to define quality KPIs and track pipeline health

  • Help maintain and improve documentation for existing data systems, pipelines, and data sources — documenting schemas, transformation logic, and known issues

  • Assist senior engineers with debugging data pipeline issues — tracing data through transformations, validating intermediate outputs, and comparing expected vs. actual results

  • Conduct quality assurance activities — reviewing data outputs, testing transformations, and validating correctness before data reaches downstream consumers

  • Perform exploratory data analysis to understand data patterns, support analytics requests, and help answer business questions about data availability and quality

  • Learn and apply data engineering best practices including version control (Git), code review processes, and testing frameworks under guidance from senior engineers

  • Support infrastructure and operational tasks as assigned — assisting with deployments, maintaining environments, and supporting on-call activities

  • Participate in knowledge-sharing and mentorship; ask questions, document learnings, and contribute to team documentation and runbooks

Required Qualifications

  • Bachelor\'s degree in Computer Science, Engineering, Information Systems, or a related field, or equivalent hands-on experience

  • Strong SQL proficiency — ability to write queries to explore, validate, and analyze data

  • Proficiency in Python or another programming language; comfort writing scripts and automation

  • Basic understanding of data modeling, ETL/ELT concepts, and data pipeline architecture

  • Familiarity with version control (Git) and collaborative development practices

  • Strong communication skills; ability to document findings clearly and ask clarifying questions

  • Analytical mindset and strong problem-solving skills, especially for data quality and debugging tasks

  • Attention to detail and commitment to data accuracy and reliability

  • Basic understanding of data quality concepts and the importance of testing and validation

  • Willingness to learn from experienced engineers and grow into a full data engineer role

Strong Pluses

  • Prior experience working with healthcare data, clinical data formats (FHIR, HL7, CCD), or claims data

  • Familiarity with cloud data platforms (AWS, Databricks, Snowflake) or data warehousing

  • Experience with dbt or other data transformation frameworks

  • Knowledge of data quality tools, monitoring, or observability platforms

  • Experience with orchestration tools (Airflow, Databricks Workflows) or workflow automation

  • Background in healthcare, pharmaceutical, or other regulated industry

  • Previous internship or project experience in data engineering or analytics

  • Familiarity with value-based care concepts, clinical workflows, or healthcare operations

  • Experience with API integration or data ingestion from external sources

  • Previous exposure to Databricks, Apache Spark, or distributed computing

  • Experience writing tests or developing QA processes for data pipelines

This job description is not designed to cover or contain a comprehensive listing of activities, duties, or responsibilities that are required of the employee. Other duties, responsibilities, and activities may change or be assigned at any time with or without notice.