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Data Coordinator I Jobs in Spring, TX (NOW HIRING)

Primary Duties & Responsibilities: • Data entry for service work and engineered product with ... Coordinator I learning path in LinkedIn Learning o Successful completion of the level I written ...

Primary Duties & Responsibilities: • Data entry for service work and engineered product with ... Coordinator I learning path in LinkedIn Learning o Successful completion of the level I written ...

HR Coordinator I

Houston, TX · On-site

$20 - $26.25/hr

NorthStar Memorial Group is seeking an HR Coordinator I at our Home Office in the Houston Galleria ... Perform basic audits of HRIS data to ensure accuracy. * Coordinate with other departments (Payroll ...

Field Count Coordinator I Location: Houston, TX (55-60% Travel Required) Company: VB Spine Looking ... Review and discuss updated inventory data with Sales Management during active counts as needed

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Data Coordinator I information

See Spring, TX salary details

$12

$23

$37

How much do data coordinator i jobs pay per hour?

As of Aug 11, 2026, the average hourly pay for data coordinator i in Spring, TX is $23.79, according to ZipRecruiter salary data. Most workers in this role earn between $18.61 and $27.40 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Data Coordinator I?

To thrive as a Data Coordinator I, you need strong organizational skills, attention to detail, and a foundational understanding of data management, typically supported by a bachelor's degree in a related field. Familiarity with database systems, Microsoft Excel, and data entry software is commonly required, and knowledge of regulatory compliance like HIPAA may be important depending on the industry. Effective communication, problem-solving abilities, and teamwork are crucial soft skills for managing information flow and collaborating with various stakeholders. These competencies ensure accurate data handling, regulatory compliance, and efficient support of organizational goals.

What are some of the typical challenges a Data Coordinator I might face during data collection and entry processes?

As a Data Coordinator I, you may often encounter challenges such as ensuring data accuracy, resolving inconsistencies, and managing incomplete or duplicate records. You'll need to pay close attention to detail while working with large datasets and be proactive in communicating with team members to clarify data issues. Balancing multiple data entry tasks under tight deadlines is also common, so strong organizational skills and familiarity with data management tools can help you succeed in this role.

What does a Data Coordinator I do?

A Data Coordinator I is responsible for collecting, organizing, and managing data within an organization. They ensure data accuracy, maintain databases, and may assist in data entry, reporting, and quality control tasks. Typically, they work with other team members to support data-related projects and help ensure that information is up-to-date and accessible for decision-making. This entry-level role often requires attention to detail, strong organizational skills, and proficiency with spreadsheet or database software.
What job categories do people searching Data Coordinator I jobs in Spring, TX look for? The top searched job categories for Data Coordinator I jobs in Spring, TX are:
What cities near Spring, TX are hiring for Data Coordinator I jobs? Cities near Spring, TX with the most Data Coordinator I job openings:
Infographic showing various Data Coordinator I job openings in Spring, TX as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 13% Part Time, and 3% Contract. Highlights an 86% Physical, 4% Hybrid, and 10% Remote job distribution, with an average salary of $49,484 per year, or $23.8 per hour.

$21 - $27.75/hr

Full-time

Re-posted 28 days ago


Job description

Clinic Research Coordinator II
The Clinical Research Coordinator I, will ensure that quality research is conducted at the assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide the best quality data to the sponsor. The CRC I will also ensure study enrollment meets or exceeds Sponsors' expectations. To ensure company goals are achieved on a timely basis.
Duties amp; Responsibilities:
  • Completing all the DMCR-required training, including but not limited to ICH-GCP Certification and IATA Certification on a timely basis.
  • Completing all the relevant training prior to study-start and on a continued basis in a timely manner. This will include but is not limited to:
    • a. Sponsor-provided and IRB-approved Protocol Training
    • b. All relevant Protocol Amendments Training
    • c. Any study-specific Manuals Training, as applicable
    • d. Sponsor-specified EDC and/or IVRS and any other relevant Electronic Systems training.
  • Conducting study subject visits, and all other relevant protocol-required procedures and documenting these in a timely manner.
  • Adherence to ALCOA-C Standards with all the relevant clinical trial documentation.
  • Completing data entry and query resolution in a timely manner as per internal company guidelines and as per sponsor expectations.
  • Demonstration of appropriate and timely follow-up on the action items, at their respective sites.
  • Demonstrated understanding and implementation of Laboratory Manuals and protocol-specified laboratory procedures, storage, temperature monitoring, equipment calibration and laboratory kit inventory, under the direction of the Site/Study Management Team, for assigned protocols.
  • Liaising with Laboratory team, Data team, Administrative staff, Clinical Investigators, Research Participants and Sponsor/CRO representatives, under the direction of the Site/Study Management Team, for assigned protocols.
  • Submitting required administrative paperwork per company timelines.
  • Participating in subject recruitment and retention efforts.
  • Engaging with Research Participants and understanding their concerns.
  • Any other matters, as assigned by management.

Knowledge amp; Experience:
Education:
  • High School Diploma or equivalent required
  • Bachelor's degree a plus
  • Foreign Medical Graduates preferred
Experience:
  • At least one years of experience as a CRC, preferably with practice coordinating industry-sponsored vaccines in a private setting.
  • At least two years of experience as a research assistant, data coordinator, laboratory personnel, or equivalent experience in a clinical research setting
Credentials:
  • ACRP or equivalent certification is preferred
  • Registered Medical Assistant certification or equivalent is preferred
  • Knowledge and Skills:
  • Be an energetic, go-getter who is detail-oriented and can multi-task.
  • Be goals-driven while continuously maintaining quality.
  • Bilingual in Spanish is preferred