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Query Processing Jobs in Belleville, MI (NOW HIRING)

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Power BI & Analytics Intern

Ann Arbor, MI · On-site

Contribute to data pipelines, ETL processes, and automation efforts under guidance from senior BIS ... Exposure to Power Query (M) and intermediate DAX measures. * Familiarity with ETL concepts, data ...

Conclusive Marketing

Senior Data Analyst

Dearborn, MI · On-site

$79K - $99K/yr

Leverage strong data wrangling skills to query, join, and manipulate large datasets, create calculated variables, and automate data processes. * Analyze business and marketing program performance ...

OneMagnify

Senior Data Analyst

Dearborn, MI · On-site

$79K - $99K/yr

Leverage strong data wrangling skills to query, join, and manipulate large datasets, create calculated variables, and automate data processes. * Analyze business and marketing program performance ...

FastTek

Platform Engineer

Dearborn, MI

Big Query * Big Data Skills Preferred: * Design and Build Data Pipelines: Architect, develop, and maintain scalable data pipelines and microservices that support real-time and batch processing on GCP.

OneMagnify

Senior Data Analyst

Dearborn, MI · On-site

$79K - $99K/yr

Leverage strong data wrangling skills to query, join, and manipulate large datasets, create calculated variables, and automate data processes. * Analyze business and marketing program performance ...

Stefanini Group

GCP Data Engineer

Dearborn, MI · On-site

Lead adoption of Gemini Enterprise for query generation, debugging, and schema optimization ... We will also speak with you about the process, including interviews and job offers. About Stefanini ...

Stefanini Group

GCP Data Engineer

Dearborn, MI · On-site

Lead adoption of Gemini Enterprise for query generation, debugging, and schema optimization ... We will also speak with you about the process, including interviews and job offers. About Stefanini ...

Stefanini Group

GCP Data Engineer

Dearborn, MI · On-site

Lead adoption of Gemini Enterprise for query generation, debugging, and schema optimization ... We will also speak with you about the process, including interviews and job offers. About Stefanini ...

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Query Processing information

See Belleville, MI salary details

$8

$15

$24

How much do query processing jobs pay per hour?

As of Sep 15, 2026, the average hourly pay for query processing in Belleville, MI is $15.75, according to ZipRecruiter salary data. Most workers in this role earn between $12.64 and $18.08 per hour, depending on experience, location, and employer.

What is query processing?

Query processing refers to the series of steps a database management system (DBMS) takes to interpret and execute a user's query. This process involves parsing the query, translating it into a suitable internal representation, optimizing it for efficient execution, and finally retrieving the requested data from the database. Effective query processing is crucial for ensuring fast and accurate results, especially in large and complex databases. It typically includes techniques like indexing, query rewriting, and using execution plans to improve performance.

What are the key skills and qualifications needed to thrive as a query processing specialist, and why are they important?

To thrive as a Query Processing Specialist, you need a solid understanding of database management, information retrieval, and data analysis, often supported by a degree in computer science or a related field. Familiarity with SQL, search algorithms, data warehousing solutions, and query optimization tools is typically required. Strong analytical thinking, problem-solving abilities, and effective communication skills help you interpret data needs and collaborate with stakeholders. These competencies are crucial for efficiently handling and optimizing queries to ensure accurate, timely access to data and support business decision-making.

How does a query processing professional typically collaborate with database administrators and software developers?

Query Processing professionals play a vital role in optimizing how databases handle and execute queries. They work closely with database administrators to analyze performance bottlenecks, suggest indexing strategies, and ensure efficient data retrieval. Collaboration with software developers is also common, as these professionals help design application queries that are both effective and resource-efficient. This teamwork ensures that end-users receive fast, accurate results while maintaining the stability and scalability of database systems.

What is the difference between Query Processing vs Data Analyst?

AspectQuery ProcessingData Analyst
Required CredentialsKnowledge of databases, SQL, and data retrieval techniquesDegree in statistics, data science, or related fields; SQL knowledge often required
Work EnvironmentDatabase systems, data warehouses, IT departmentsBusiness environments, analytics teams, reporting tools
Industry UsageIT, software development, database managementFinance, marketing, healthcare, and other sectors relying on data insights

Query Processing focuses on retrieving and managing data efficiently within databases, often involving technical skills like SQL and database management. Data Analysts interpret data, generate reports, and provide insights for decision-making. While both roles work with data, Query Processing is more technical and system-oriented, whereas Data Analysts focus on analysis and business applications.

What are popular job titles related to Query Processing jobs in Belleville, MI?

For Query Processing jobs in Belleville, MI, the most frequently searched job titles are:

Clinical Research Coordinator II

Detroit, MI

DM Clinical Research
11 - 50 employees
Learn more about DM Clinical Researchexternal

$24 - $32/hr

Full-time

Re-posted 5 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