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Research Data Manager Jobs in Texas (NOW HIRING)

Clinical Research Coordinator

Galveston, TX · On-site

$22.75 - $30.25/hr

... manage, and safeguard research data. The CRC serves as a key liaison among research participants, investigators, sponsors, and regulatory bodies to support proper study conduct, subject safety, and ...

Clinical Research Coordinator

Galveston, TX · On-site

$22.75 - $30.25/hr

... manage, and safeguard research data. The CRC serves as a key liaison among research participants, investigators, sponsors, and regulatory bodies to support proper study conduct, subject safety, and ...

With our three market leading businesses, world-class operations and investments in research and ... Builds a data track in a Product Data Management (PDM) system * Identifies, with help from the ...

With our three market leading businesses, world-class operations and investments in research and ... Builds a data track in a Product Data Management (PDM) system * Identifies, with help from the ...

Showing results 21-40

Research Data Manager information

See Texas salary details

$28.9K

$90.5K

$160.2K

How much do research data manager jobs pay per year?

As of Aug 21, 2026, the average yearly pay for research data manager in Texas is $90,505.00, according to ZipRecruiter salary data. Most workers in this role earn between $61,500.00 and $116,900.00 per year, depending on experience, location, and employer.

What is a research data manager?

Research Data Managers are professionals responsible for overseeing the collection, organization, storage, and sharing of research data throughout the lifecycle of a research project. They ensure data integrity, security, and compliance with relevant legal, ethical, and institutional requirements. Their work enables researchers to manage data efficiently, promote data sharing, and support reproducibility and transparency in research.

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

To thrive as a Research Data Manager, you need expertise in data management, database design, and knowledge of regulatory compliance, often supported by a degree in information science or a related field. Familiarity with data management systems (such as REDCap or SQL databases), data security protocols, and relevant certifications like Certified Research Data Manager (CRDM) is typically required. Strong organizational skills, attention to detail, and effective communication are vital soft skills for coordinating with research teams and ensuring data integrity. These abilities ensure that research data is accurate, secure, and accessible, supporting the success and credibility of scientific projects.

What are some common challenges faced by research data managers, and how can they be addressed in day-to-day work?

Research Data Managers often encounter challenges such as ensuring data integrity, managing large volumes of diverse data, and complying with data privacy regulations. To address these issues, they implement robust data management plans, maintain clear documentation, and regularly conduct data audits. Effective collaboration with researchers and IT staff is also essential to streamline workflows and troubleshoot data-related issues, ensuring the research process remains efficient and compliant.

What is the difference between Research Data Manager vs Data Analyst?

AspectResearch Data ManagerData Analyst
Required CredentialsBachelor's or Master's in Data Science, Information Management, or related fieldsBachelor's or Master's in Statistics, Data Science, or related fields
Work EnvironmentResearch institutions, universities, clinical trials, or research labsBusiness, finance, marketing, or healthcare organizations
Employer & Industry UsagePrimarily in research settings managing data collection, storage, and complianceAnalyzing data to inform business decisions across various industries

Research Data Managers focus on organizing, maintaining, and ensuring the integrity of research data within academic or clinical research environments. Data Analysts interpret and analyze data to generate insights for business or research purposes. While both roles require strong data skills, Research Data Managers emphasize data management and compliance, whereas Data Analysts focus on data interpretation and reporting.

What are the most commonly searched types of Research Data jobs in Texas?

The most popular types of Research Data jobs in Texas are:

What cities in Texas are hiring for Research Data Manager jobs?

Cities in Texas with the most Research Data Manager job openings:

Infographic showing various Research Data Manager job openings in Texas as of August 2026, with employment types broken down into 89% Full Time, 10% Part Time, and 1% Contract. Highlights an 81% Physical, 2% Hybrid, and 17% Remote job distribution, with an average salary of $90,505 per year, or $43.5 per hour.

Clinical Research Coordinator

Shriners Children's

Galveston, TX • On-site

$22.75 - $30.25/hr

Full-time

Re-posted 5 days ago


Shriners Children's rating

8.0

Company rating: 8.0 out of 10

Based on 45 frontline employees who took The Breakroom Quiz

137th of 1,061 rated hospitals


Job description

Company Overview
Shriners Children's is an organization that respects, supports, and values each other. Named as the 2025 best mid-sized employer by Forbes, we are engaged in providing excellence in patient care, embracing multi-disciplinary education, and research with global impact. We foster a learning environment that values evidenced based practice, experience, innovation, and critical thinking. Our compassion, integrity, accountability, and resilience define us as leaders in pediatric specialty care for our children and their families.
With 20+ hospitals, outpatient clinics, ambulatory care centers and outreach locations across the globe, we provide excellent care to children up to age 18 regardless of their family's ability to pay or insurance status. Please click here to learn more about our locations.
Job Description
The Clinical Research Coordinator, Level 1 (CRC I) is a research professional responsible for supporting the oversight and compliance of both system-wide and local Shriners Children's (SHC) clinical research activities. Reporting to the Clinical Research Program Manager (or local Hospital Administrator/Clinic Director) and collaborating with the Research Programs Office at SHC International Headquarters, the CRC provides support in accordance with SHC policies and procedures, hospital regulations, the Code of Federal Regulations, and Good Clinical Practice (GCP) guidelines, when applicable.
The CRC works collaboratively with investigators, research staff, and clinical teams to ethically recruit and consent Shriners Children's vulnerable pediatric research participants and to appropriately collect, manage, and safeguard research data. The CRC serves as a key liaison among research participants, investigators, sponsors, and regulatory bodies to support proper study conduct, subject safety, and the quality and integrity of study data.
Key Responsibilities:
  • Supports the implementation and conduct of approved research protocols, ensuring studies are performed in compliance with the protocol, Good Clinical Practice (GCP), applicable regulatory requirements, and SHC policies and standards.
  • Performs study-specific research activities and/or interventions within the bounds of professional licensure and training.
  • Assists with participant recruitment, screening, informed consent/assent, scheduling, and coordination of study visits.
  • Coordinates the collection and documentation of research data.
  • Maintains regulatory documentation and study records in accordance with institutional policies and sponsor requirements.
  • Supports communication and coordination between investigators, sponsors, monitors, and institutional departments involved in research activities.
  • Assists investigators with the development and submission of investigator-initiated research protocols and related regulatory documentation.
  • Contributes to study progress reports, monitoring visits, audits, and preparation of study results or presentations when applicable.
  • Ensures appropriate training and education are completed in order to safely perform study-related procedures and protocol requirements.

Required Qualifications:
  • 1 or more years of relevant research experience (e.g., study coordination, site management, regulatory submissions, or clinical data management)

Preferred Qualifications:
  • Bachelor's degree in Clinical Research, Life Sciences, Public Health, or another healthcare-related field
  • Working knowledge of regulations and guidance related to clinical research (e.g., GCP, FDA regulations, IRB requirements)
  • Experience coordinating intergroup or multi-site clinical studies
  • CCRP or CCRC certification
Compensation is determined based on years of relevant experience and departmental equity.

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