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Clinical Data Manager Jobs in Rosharon, TX (NOW HIRING)

Shriners Children's

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 ...

CenterWell

Clinical Care Nurse - Houston

Houston, TX · On-site

The Clinical Care RN plays a critical role in advancing clinical quality and supporting patients ... management. * Proficiency with electronic health records (e.g., Athena EMR), data analytics tools ...

Tranquil Clinical Research

Research Intern

Webster, TX · On-site

Maintain confidentiality of data, as required. * Plan, conduct and manage research projects ... Enter clinical and research data and information into database, include electronic CRFs and sample ...

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How much do clinical data manager jobs pay per hour?

As of Aug 23, 2026, the average hourly pay for clinical data manager in Rosharon, TX is $51.15, according to ZipRecruiter salary data. Most workers in this role earn between $40.43 and $60.87 per hour, depending on experience, location, and employer.

What does a clinical data manager do?

A Clinical Data Manager is responsible for collecting, validating, and managing data from clinical trials to ensure its accuracy, integrity, and compliance with regulatory standards. They design data collection systems, oversee database development, and collaborate with clinical research teams to resolve data discrepancies. By ensuring high-quality data, Clinical Data Managers play a vital role in the success of clinical trials and the development of new medical treatments.

What does a clinical data manager do?

A clinical data manager handles all the data needs of clinical trials for biotechnology and pharmaceutical companies. As a clinical data manager, your responsibilities include the research and storage of data related to clinical trials and programs. Your job duties are to collect, process, and analyze data. You must routinely evaluate your data collection and analysis processes to ensure that results are accurate and valid. You must also ensure that your work is in compliance with ethical research standards and regulations from organizations like the Food and Drug Administration (FDA).

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

To thrive as a Clinical Data Manager, you need a solid understanding of clinical research processes, data management principles, and a degree in life sciences, computer science, or related fields. Expertise with clinical data management systems (CDMS), electronic data capture (EDC) tools, and familiarity with regulatory standards like CDISC and GCP are typically required. Attention to detail, problem-solving abilities, and effective communication distinguish top performers in this role. These skills ensure accurate, compliant data handling and seamless collaboration across clinical research teams, which are critical for successful clinical trial outcomes.

What are some common challenges clinical data managers face when working on multi-site clinical trials?

Clinical Data Managers often encounter challenges such as ensuring data consistency across different sites, managing large volumes of complex data, and coordinating with site staff to resolve discrepancies. They must also stay up-to-date with regulatory requirements and ensure timely data cleaning and database lock. Effective communication and strong organizational skills are essential to navigate these complexities and maintain high data quality throughout the study.

How much do clinical data managers make in the US?

Clinical data managers in the US typically earn between $70,000 and $110,000 annually, with salaries varying based on experience, education, and location. Entry-level positions may start around $60,000, while experienced professionals with specialized skills can earn over $120,000. Certifications in data management and proficiency with electronic data capture systems can also influence salary levels.
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Clinical Data Manager jobs near you
Infographic showing various Clinical Data Manager job openings in Rosharon, TX as of August 2026, with employment types broken down into 82% Full Time, 15% Part Time, 2% Temporary, and 1% Contract. Highlights an 81% Physical, 2% Hybrid, and 17% Remote job distribution, with an average salary of $106,396 per year, or $51.2 per hour.

Clinical Research Coordinator

Shriners Children's

Galveston, TX • On-site

$22.75 - $30.25/hr

Full-time

Re-posted 7 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

136th of 1,062 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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