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Clinical Data Associate Jobs in Spring, TX (NOW HIRING)

Deloitte

Senior Manager Data Lead

Houston, TX

Work You'll Do As an Associate Vice President, AI and Data Solutions on the AI & Data team, you ... Clinical data exchange and coding standards, including HL7, FHIR, and ICD * Data operations (ie ...

Theravolve

Clinic Director PT [PT Associates]

Conroe, TX · On-site

$90 - $100/hr

At PT Associates, we believe great clinicians do not need to be managed. They need clarity ... Progress treatment plans based on patient response and clinical data * Ensure a consistent, high ...

Immatics NV

Senior Clinical Research Associate

Houston, TX · On-site

$120K - $135K/yr

Associate Director, Team Lead Site Operations Location : Fully Remote Salary Range: $120,000 to ... Strong understanding of clinical trial recruitment strategies, data capture, and site engagement ...

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All JobsClinical Data Associate JobsClinical Data Associate Jobs in Spring, TX

Clinical Data Associate information

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How much do clinical data associate jobs pay per hour?

As of Sep 3, 2026, the average hourly pay for clinical data associate in Spring, TX is $34.66, according to ZipRecruiter salary data. Most workers in this role earn between $26.11 and $34.66 per hour, depending on experience, location, and employer.

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 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.

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 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.

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.

More about Clinical Data Associate jobs

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Clinical Data Associate jobs near you
Infographic showing various Clinical Data Associate job openings in Spring, TX as of August 2026, with employment types broken down into 1% As Needed, 84% Full Time, 12% Part Time, and 3% Contract. Highlights an 84% Physical, 4% Hybrid, and 12% Remote job distribution, with an average salary of $72,099 per year, or $34.7 per hour.

Postdoctoral Associate - Bioinformatics

Baylor College of Medicine

Houston, TX • On-site

$62K - $65K/yr

Full-time

Re-posted 27 days ago

Baylor College of Medicine rating

8.0

Company rating: 8.0 out of 10

Based on 24 frontline employees who took The Breakroom Quiz

190th of 628 rated colleges and universities

Job description

Postdoctoral Associate - Bioinformatics
Division: Pediatrics
Work Arrangement: Onsite only
Location: Houston, TX
Salary Range: $62,232 - $65,000
FLSA Status: Exempt
Work Schedule: Monday - Friday, 8 a.m. - 5 p.m.
Summary
Baylor College of Medicine is seeking a highly motivated Postdoctoral Research Associate for an integrative analysis of transcriptomic, epigenomic, and proteomic large-scale datasets, under the joint supervision of Dr. Cristian Coarfa and Dr. Andrew DiNardo. This is an opportunity for an ambitious scientist committed to advancing their academic career, who demonstrates strong work ethic, exceptional initiative, and an innovative, analytical approach to solving complex scientific problems. The position will involve analysis of DNA methylation, single cell RNA and ATAC sequencing, Fiber-sequencing, and data science approaches to support research aimed at understanding long-term molecular changes induced by infections, in particular tuberculosis and other respiratory infections.
Baylor College of Medicine typically follows similar to the NIH stipulated stipend guidelines for Postdoctoral Associates.
Job Duties
  • Analyzes single cell RNA-Sequencing, single cell ATAC-Seq, CITE-Seq, as well as bulk RNA-Seq, Proteomics, Metabolomics, and other datasets, generated from tuberculosis patient cohorts with rich clinical data.
  • Performs advanced modeling of post-tuberculosis lung disease risk using approaches including generalized linear models and deep learning.
  • Performs other job-related duties as assigned.

Minimum Qualifications
  • MD or Ph.D. in Basic Science, Health Science, or a related field.
  • No experience required.

Preferred Qualifications
  • Ph.D. in Computer Science, Bioinformatics, or Biology, with a strong background in statistics and familiarity with large datasets such as proteomics or sequencing.
  • Experience in epigenetics or gene regulation is a plus.
  • Experience with statistical analysis tools such as R or Python is required (Candidates will be expected to pass a basic programming test in Python).
  • Excellent written and verbal English skills, strong communication and interpersonal skills, and the ability to work within large collaborative teams.

Requisition ID: 25797

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