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Data Entry Research Jobs in Spring, TX (NOW HIRING)

CBG Surveying Texas

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Access Coordinator / Data Entry

Houston, TX · On-site

Support Customer Service, Research, Scheduling, Sales and Operations teams with administrative tasks as needed. Property Access Coordination * Serve as the initial point of contact for property ...

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Data Entry Research information

See Spring, TX salary details

$9

$17

$25

How much do data entry research jobs pay per hour?

As of Jun 22, 2026, the average hourly pay for data entry research in Spring, TX is $17.33, according to ZipRecruiter salary data. Most workers in this role earn between $14.57 and $19.47 per hour, depending on experience, location, and employer.

What is the highest paying data entry job?

The highest paying data entry roles typically involve specialized skills such as medical or legal transcription, data management, or roles requiring proficiency in advanced software and database systems. These positions can offer higher salaries, especially with experience, certifications, or working for large organizations, but generally, data entry jobs have modest pay compared to other data-related roles.

What is a Data Entry Research job?

A Data Entry Research job involves collecting, organizing, and inputting data into databases, spreadsheets, or other digital systems. Professionals in this role verify accuracy, maintain data integrity, and may also conduct basic research to gather missing or relevant information. They often work with large datasets, ensuring that information is up-to-date and correctly formatted. This role is critical in various industries, including healthcare, finance, and marketing, where accurate data is essential for decision-making. Strong attention to detail, typing skills, and familiarity with data management tools are key for success in this position.

Do you need a PhD to be a research assistant?

A PhD is generally not required to be a research assistant; most positions require a bachelor's degree or equivalent in a relevant field. Advanced degrees may be preferred for research roles involving complex data analysis or specialized research, but entry-level research assistant positions typically focus on skills like data entry, research, and familiarity with tools such as spreadsheets or databases.

What are the key skills and qualifications needed to thrive in the Data Entry Research position, and why are they important?

To thrive as a Data Entry Research professional, you need excellent attention to detail, fast and accurate typing skills, and experience with data management or research tools. Familiarity with spreadsheet applications (like Microsoft Excel or Google Sheets), database software, and sometimes data analysis platforms is often required. Strong organizational abilities, problem-solving skills, and the capacity to work independently or as part of a team are highly valued. These skills are vital for ensuring data accuracy, efficiency in research processes, and supporting decision-making within an organization.

What is research data entry?

Research data entry involves inputting, organizing, and managing data collected from research studies into digital formats or databases. It requires attention to detail, accuracy, and often the use of data management tools or software to ensure data integrity for analysis and reporting.

How can I make $2000 a week working from home?

Data Entry Research roles typically pay hourly or per project, and earning $2000 weekly requires high-volume work or premium rates, which are uncommon in standard data entry positions. To increase earnings, professionals often need advanced skills, efficient use of data management tools, and the ability to handle multiple projects simultaneously, but consistent high weekly income is challenging without specialized expertise or additional income streams.

What are the typical daily tasks for someone working in Data Entry Research?

Professionals in Data Entry Research spend most of their day gathering, entering, and validating large amounts of data from various sources, ensuring accuracy and consistency. They may also use online databases, spreadsheets, and research tools to organize information and generate basic reports for stakeholders. Collaboration with other departments, such as marketing or analytics teams, is common to clarify data needs and resolve discrepancies. This role often requires a balance between independent focus and working within a structured team environment, making effective communication and time management essential.

What are popular job titles related to Data Entry Research jobs in Spring, TX? For Data Entry Research jobs in Spring, TX, the most frequently searched job titles are:
What job categories do people searching Data Entry Research jobs in Spring, TX look for? The top searched job categories for Data Entry Research jobs in Spring, TX are:
What cities near Spring, TX are hiring for Data Entry Research jobs? Cities near Spring, TX with the most Data Entry Research job openings:
Data Entry Research jobs near you
Infographic showing various Data Entry Research job openings in Spring, TX as of June 2026, with employment types broken down into 1% Locum Tenens, 1% As Needed, 85% Full Time, 12% Part Time, and 1% Contract. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $36,044 per year, or $17.3 per hour.
Clinical Research Coordinator II

Clinical Research Coordinator II

DM Clinical Research

Humble, TX

$21 - $27.75/hr

Full-time

Posted 12 days ago

Job description

Clinical Research Coordinator II
The Clinical Research Coordinator II, 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 II 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:
    • Sponsor-provided and IRB-approved Protocol Training
    • All relevant Protocol Amendments Training
    • Any study-specific Manuals Training, as applicable
    • 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 the 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.
  • Demonstrating adherence and compliance to the assigned protocols at their respective site(s).
  • Maintaining a working knowledge of current FDA regulations, ICH-GCP guidelines, all the organizational SOPs, all the guidance documents, and assigned study protocol(s)
  • Maintaining a working knowledge of the recruitment and retention process for their assigned protocol(s) at their respective site(s).
  • Demonstrating visit preparedness for all the relevant sponsor and CRO visits for their assigned protocol(s)
  • Demonstration of appropriate and timely follow-up on the action items, at their respective sites.
  • Maintaining a working knowledge of the most recent versions of the Study Protocols, Informed consents, Study Manuals, and all the other relevant study-related documents that are utilized and implemented for the assigned protocols at their respective site(s).
  • Oversee reporting of all Adverse and Serious Adverse Events and any other relevant Safety Information to the appropriate authorities per internal company guidelines, Sponsor, IRB, and ICH-GCP Guidelines.
  • Completing data entry and query resolution in a timely manner as per internal company guidelines and as per sponsor expectations.
  • Striving to meet Sponsor subject enrollment goals for their assigned protocols at their respective site(s).
  • Being prepared for and available at all required company meetings.
  • Submitting required administrative paperwork per company timelines.
  • Occasionally attending out-of-town Investigator Meetings
  • Any other matters as assigned by management.
Knowledge amp; Experience:

Education:
  • High School Diploma or equivalent required
  • Bachelor's degree a preferred
  • Foreign Medical Graduates preferred
Experience:
  • At least 2 years of experience as a CRC, preferably with practice coordinating industry-sponsored vaccines in a private setting.
Credentials:
  • ACRP or equivalent certification 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 a plus

Apply