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Data Coordinator I Jobs in Romeoville, IL (NOW HIRING)

HR Data Coordinator/Assistant

Chicago, IL · On-site

$38K - $49K/yr

Maintain employee files, prepare HR correspondence, process mail, and manage I-9s. * Serve as the ... Payroll verification of system transactions for data accuracy (pay, job titles, etc) * Complete ...

We are looking for a Pathology Lab Coordinator who will be responsible for the coordination between ... Abstract clinical data accurately and efficiently from patient documents * Support multiple ...

CLINICAL RESEARCH COORDINATOR I

Chicago, IL · Hybrid

$25 - $33.25/hr

As a Moffitt Clinical Research Coordinator, you'll bring hope to patients by delivering tomorrow ... Responsible for data and source documentation and adverse experience reporting. Perform diverse ...

CLINICAL RESEARCH COORDINATOR I

Chicago, IL · Hybrid

$26.32 - $40.14/hr

As a Moffitt Clinical Research Coordinator, you'll bring hope to patients by delivering tomorrow ... Responsible for data and source documentation and adverse experience reporting. Perform diverse ...

We are looking for a Pathology Lab Coordinator who will be responsible for the coordination between ... Abstract clinical data accurately and efficiently from patient documents * Support multiple ...

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Data Coordinator I information

See Romeoville, IL salary details

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$27

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How much do data coordinator i jobs pay per hour?

As of Aug 25, 2026, the average hourly pay for data coordinator i in Romeoville, IL is $27.26, according to ZipRecruiter salary data. Most workers in this role earn between $21.35 and $31.39 per hour, depending on experience, location, and employer.

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 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.

How much does a data coordinator I make?

The average salary for a Data Coordinator I in Texas is approximately $40,000 to $50,000 per year, depending on experience, industry, and location. Entry-level roles typically require basic data management skills and familiarity with tools like Excel or database systems.

Is a data coordinator I an entry level position?

A Data Coordinator I is typically an entry-level position that involves basic data management tasks, data entry, and supporting data quality efforts. It often requires little to no prior experience and may involve learning tools like spreadsheets or database software as part of the role.

What are popular job titles related to Data Coordinator I jobs in Romeoville, IL?

For Data Coordinator I jobs in Romeoville, IL, the most frequently searched job titles are:

What job categories do people searching Data Coordinator I jobs in Romeoville, IL look for?

The top searched job categories for Data Coordinator I jobs in Romeoville, IL are:

What cities near Romeoville, IL are hiring for Data Coordinator I jobs?

Cities near Romeoville, IL with the most Data Coordinator I job openings:

Infographic showing various Data Coordinator I job openings in Romeoville, IL as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 15% Part Time, 1% Temporary, and 3% Contract. Highlights an 84% Physical, 4% Hybrid, and 12% Remote job distribution, with an average salary of $56,697 per year, or $27.3 per hour.

Clinical Research Coordinator I

DM Clinical Research

Chicago, IL

$25 - $33.25/hr

Full-time

Re-posted 17 days ago


Job description

Clinical Research Coordinator I
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