ZipRecruiter

Log In

1

Research Data Associate Jobs in Beaumont, TX (NOW HIRING)

Walmart

Vision Center Manager NL 1

Beaumont, TX · On-site

... with Associates and listening to concerns researching issues reviewing Company policies and ... data insights and analysis balances short and longterm priorities and considers our customers ...

next page

Showing results 1-20

All JobsResearch Data Associate JobsResearch Data Associate Jobs in Beaumont, TX

Research Data Associate information

See Beaumont, TX salary details

$15

$31

$44

How much do research data associate jobs pay per hour?

As of Aug 22, 2026, the average hourly pay for research data associate in Beaumont, TX is $31.17, according to ZipRecruiter salary data. Most workers in this role earn between $25.10 and $35.48 per hour, depending on experience, location, and employer.

What is a research data associate?

Research Data Associates are professionals who support research projects by managing, analyzing, and interpreting data. They are responsible for collecting data, ensuring its quality, maintaining databases, and preparing reports or summaries for research teams. Their work is essential in academic, medical, or industrial research settings, where accurate and reliable data is crucial for decision-making and publication. Research Data Associates often collaborate with researchers, statisticians, and IT staff to ensure data integrity and security.

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

To thrive as a Research Data Associate, you generally need strong quantitative analysis skills, attention to detail, and a relevant bachelor's degree in fields like statistics, data science, or a related discipline. Familiarity with data management tools such as SQL, SPSS, R, or Python, as well as experience with data collection and cleaning processes, is typically required. Effective communication, problem-solving, and collaboration skills help Research Data Associates work efficiently within research teams and convey findings clearly. These competencies ensure accurate data handling, meaningful analysis, and the reliability of research outcomes.

What are some common challenges research data associates face when managing large datasets, and how can they be addressed?

Research Data Associates often encounter challenges such as ensuring data quality, maintaining accurate documentation, and handling missing or inconsistent data within large datasets. To address these, they typically implement rigorous data cleaning protocols, work closely with research teams to standardize data collection processes, and use specialized software for data validation. Collaborating with statisticians and IT staff is also essential to resolve technical issues and maintain data integrity throughout the project lifecycle.

What cities near Beaumont, TX are hiring for Research Data Associate jobs?

Cities near Beaumont, TX with the most Research Data Associate job openings:

Research Data Associate jobs near you
Infographic showing various Research Data Associate job openings in Beaumont, TX as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 14% Part Time, and 4% Contract. Highlights an 86% Physical, 4% Hybrid, and 10% Remote job distribution, with an average salary of $64,843 per year, or $31.2 per hour.

Clinical Research Coordinator I - Port Arthur, TX

Iterative Health

Port Arthur, TX • On-site

$20.50 - $27.25/hr

Full-time

Re-posted 25 days ago

Job description

We are seeking a full-time, experienced Clinical Research Coordinator (CRC). The CRC supports, facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study.  

Responsibilities:

  • Administratively and clinically manage industry-sponsored clinical trials including problem solving, communication and protocol management. 
  • Lead patient recruitment activities, e.g., performing chart reviews, discussing protocols with patients, and verifying the informed consent documentation
  • Schedule all patient research visits and procedures consistent with protocol requirements
  • Conduct patient visits as outlined within each study protocol
  • Dispense study medication, collect vital signs and perform ECGs
  • Perform blood draws, process and ship specimens per study protocol and IATA regulations
  • Ensure relevant study and subject specific information is entered into the CTMS system  on a regular basis; complete and maintain documentation study files including, but not limited to, consent forms, source documentation, progress notes if applicable, case report forms, and investigational accountability forms. 
  • Act as point of contact for study participants
  • Adhere to Research SOPs, Good Clinical Practices, and the study protocols
  • Maintain ongoing communication with the CRO, sponsor, research participants, Site  Manager and PI throughout course of the study
  • Ensure all safety data is reviewed by the PI in a timely manner 
  • Maintain inventory of study equipment and supplies onsite at all times
  • Participate actively in communication of status and results to management 
  • Assist with routine data verification and quality control, ensuring data integrity and consistency with prescribed study protocol
  • Schedule and prepare for monitor visits
  • Assists Study Team in protection of the rights and welfare of all human research participants involved in research in accordance with Federal regulations
  • Cooperates with site compliance and monitoring efforts regarding the access, use, and disclosure of PHI and reports instances of noncompliance 
  • Complete and maintain case report forms per FDA guidelines, and review them against the patient's medical record for completeness and accuracy

Iterative Health Expectations

All employees are expected to:  

  • Perform quality work within deadlines with or without direct supervision
  • Interact professionally with other employees, customers and suppliers
  • Work effectively as a team contributor on all assignments
  • Work independently while understanding the necessity for communicating and  coordinating work efforts with other employees and organizations

Qualifications

  • Medical Assistant, LPN, Associates or Bachelor's degree in a clinical or scientific-related discipline preferred
  • Minimum 1-2 years of clinical research experience
  • Able to execute on research tasks with guidance from more experienced staff, PIs, and management
  • Strong written and verbal communication skils
  • Ability to read, interpret, and apply clinic policies and research protocols
  • Ability to use standard office software
  • Must be able to lift up to 25 pounds

At Iterative Health, we're actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.

Apply