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Clinical Research Data Assistant Jobs (NOW HIRING)

Clinical Research Data Assistant Role in Lakewood, CO Job Summary As a Data Entry Clerk, you will be instrumental in upholding the accuracy and quality of clinical research data at our oncology sites.

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How much do clinical research data assistant jobs pay per hour?

As of Aug 12, 2026, the average hourly pay for clinical research data assistant in the United States is $22.71, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $25.96 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a clinical research data assistant?

To thrive as a Clinical Research Data Assistant, you need strong attention to detail, data entry accuracy, familiarity with clinical research protocols, and typically an associate’s or bachelor’s degree in a health-related or scientific field. Proficiency in data management systems such as REDCap, EDC platforms, and Microsoft Excel, as well as knowledge of Good Clinical Practice (GCP) guidelines, is often required. Strong organizational skills, clear communication, and the ability to collaborate with research teams make candidates stand out. These skills ensure careful handling of sensitive data, regulatory compliance, and efficient support for clinical research studies.

What does a clinical research data assistant do?

A Clinical Research Data Assistant is responsible for managing and organizing data collected during clinical trials and research studies. They ensure the accuracy, integrity, and confidentiality of data by entering, verifying, and maintaining research records. These professionals also assist with data cleaning, preparing reports, and supporting regulatory compliance. Their work is essential for the successful analysis and reporting of clinical research findings.

What are some typical challenges faced by clinical research data assistants in maintaining data accuracy?

Clinical Research Data Assistants often encounter challenges such as managing large volumes of complex data, ensuring accurate data entry from multiple sources, and adhering to strict regulatory standards. Mistakes can occur if data is not consistently verified or if communication between research teams is lacking, so attention to detail and strong organizational skills are essential. Regular audits, clear documentation procedures, and collaboration with clinical coordinators help address these challenges and maintain data integrity throughout the research process.

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

AspectClinical Research Data AssistantClinical Research Coordinator
CredentialsTypically requires a high school diploma or associate degree; some roles prefer certification in clinical researchRequires a bachelor's degree, often in health sciences or related field; certification like CCRP is common
Work EnvironmentSupports data entry, management, and documentation in clinical trial settingsManages entire study processes, including patient recruitment, compliance, and coordination
Employer & IndustryHospitals, research institutions, pharmaceutical companiesResearch sites, hospitals, academic institutions

The Clinical Research Data Assistant primarily handles data-related tasks within clinical trials, while the Clinical Research Coordinator oversees the entire study process. Both roles are essential in clinical research but differ in responsibilities and required qualifications.

More about Clinical Research Data Assistant jobs
What cities are hiring for Clinical Research Data Assistant jobs? Cities with the most Clinical Research Data Assistant job openings:
What are the most commonly searched types of Clinical Research Data jobs? The most popular types of Clinical Research Data jobs are:
What states have the most Clinical Research Data Assistant jobs? States with the most job openings for Clinical Research Data Assistant jobs include:
Infographic showing various Clinical Research Data Assistant job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 84% Full Time, 11% Part Time, and 4% Contract. Highlights an 86% Physical, 4% Hybrid, and 10% Remote job distribution, with an average salary of $47,241 per year, or $22.7 per hour.

Clinical Research Data Assistant

Medix

Denver, CO • On-site

$43K - $54K/yr

Full-time

This job post has expired today. Applications are no longer accepted.


Job description

Clinical Research Data Assistant Role in Lakewood, CO

Job Summary

As a Data Entry Clerk, you will be instrumental in upholding the accuracy and quality of clinical research data at our oncology sites. Your primary focus will be inputting, maintaining, and verifying patient and clinical information within Electronic Data Capture (EDC) platforms and clinical data systems. You will ensure all data strictly matches source documents, quickly address any inconsistencies, and guarantee that all records are comprehensive, secure, and fully compliant with GCP, HIPAA, regulatory guidelines, and internal protocols.

Position Details

  • Location: Lakewood, CO (80228)

  • Schedule: Monday-Friday; Normal Business Hours; Onsite 5 days a week

  • Compensation: $21.00/hr-$26.00/hr ($43,680-$54,080 Annual Salary) - Dependent on experience

Key Responsibilities

  • Accurately input clinical trial data into clinical data management systems (CDMS) or case report forms (CRFs), rigorously verifying it against source documentation.

  • Ensure all data entry activities adhere to Good Clinical Practice (GCP) standards.

  • Identify and help resolve data queries by flagging discrepancies between physical source files and digital entries.

  • Safeguard Protected Health Information (PHI) to maintain strict HIPAA compliance and patient confidentiality.

  • Collaborate with physicians, research coordinators, and clinical staff to facilitate data retrieval and corrections.

  • Prepare for and support audits by ensuring all documentation is accurate, complete, and properly filed.

  • Uphold data integrity across all clinical databases and registries.

  • Maintain a professional, courteous demeanor in all written, verbal, and in-person interactions with vendors, clients, and colleagues.

  • Execute all duties safely and responsibly, taking on additional administrative tasks as assigned by management.

Qualifications & Skills

  • Education: High school diploma or equivalent required. An Associate's degree (especially in Health Information Management, Medical Assisting, or a related field) is highly preferred.

  • Experience: 1 to 3 years of dedicated data entry experience. Prior experience working with healthcare, medical, or clinical trial data is strongly desired.

  • Technical Knowledge: Hands-on experience with EHR/EMR systems or clinical trial platforms, alongside a solid grasp of clinical documentation standards and medical terminology.

  • Computer Skills: Exceptional typing speed and accuracy; highly proficient in Microsoft Office Suite and web-based applications.

  • Compliance: A thorough understanding of patient confidentiality laws and HIPAA regulations.

  • Core Competencies: Highly organized with flawless attention to detail, strong problem-solving abilities, and the capacity to handle high-volume, repetitive tasks without losing focus or accuracy.

  • Communication: Excellent verbal and written communication skills.

  • Work Ethic: Dependable, adaptable, and aligned with core organizational values, demonstrating a readiness to shift priorities and take on new responsibilities as needed.

For California Applicants:

We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable federal, state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance (FCIHO), Los Angeles Fair Chance Ordinance for Employers (ULAC), The San Francisco Fair Chance Ordinance (FCO) , and the California Fair Chance Act (CFCA).

This position is subject to a background check based on its job duties, which may include patient care, working with vulnerable populations, access to financial and confidential information, driving, working with heavy machinery, or working in a warehouse or laboratory environment. Due to these job duties, this position has a significant impact on the business operations and reputation, as well as the safety and well-being of individuals who may be cared for as part of the job position or who may interact with staff or clients.

Company Description

Here at Medix, we are dedicated to providing workforce solutions to clients throughout multiple industries. We have been named among the Best and Brightest Companies to Work For in the Nation for two consecutive years. Medix has also been ranked as one of the fastest growing companies by Inc. Magazine.

Our commitment to our core purpose of positively impacting 20,000 lives affects not only the way we interact with our clients and talent, but also with our co-workers! The goal is lofty, but it is made attainable through the hard work and dedication of our teams and their willingness to lock arms together. Are you ready to lock arms with us?


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About Medix Staffing Solutions

Sourced by ZipRecruiter

Since 2001, we’ve been dedicated to helping you achieve your goals. Medix was created to become a leading provider of workforce solutions for clients and candidates across the healthcare and life sciences industries. Today, we are that leader. Headquartered in Chicago, we have 23 offices across the United States, and staff talent around the world. Medix is committed to fulfilling our core purpose as an organization: to positively impact the lives of our talent, clients, and teammates through employment, philanthropy, and opportunity. The combination of purpose and values has nurtured our thriving culture that encourages our internal team to excel at work and in everyday life.

Industry

Recruiting and staffing services

Company size

1,001 - 5,000 Employees

Headquarters location

Chicago, IL, US