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Data Collection Associate Jobs in Detroit, MI (NOW HIRING)

University of Michigan

Data Manager

Ann Arbor, MI · On-site

$32K - $37K/yr

The Data Manager supports data collection processes, reports, and tracking systems. The Data ... You will report to the Associate Director of OAMI. You will work a hybrid role in Ann Arbor. This ...

Albia Community School District, IA

Associate

Warren, MI · On-site

$13.75 - $15.75/hr

Please apply here: -5879.html Associate A special education paraprofessional assists lead teachers ... Data Collection: Record and track student progress, attendance, and behavior to assist with ...

McLaren

Administrative Assistant

Detroit, MI · On-site

$17.75 - $24/hr

... data collection methods. * Reviews and answers correspondences. Qualifications: Required: * High School Diploma * Minimum four years of clerical experience Preferred: * Associates Degree Equal ...

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Data Collection Associate information

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How much do data collection associate jobs pay per hour?

As of Aug 4, 2026, the average hourly pay for data collection associate in Detroit, MI is $20.44, according to ZipRecruiter salary data. Most workers in this role earn between $16.63 and $22.84 per hour, depending on experience, location, and employer.

What are some common challenges faced by data collection associates and how can they be managed effectively?

Data Collection Associates often encounter challenges such as ensuring data accuracy, maintaining consistency across multiple sources, and meeting tight deadlines. Effective management involves following standardized protocols, double-checking entries for errors, and using digital tools to streamline data capture. Collaborating closely with team members and supervisors can help resolve ambiguities and improve overall data quality. Regular training and feedback sessions also contribute to overcoming these challenges and enhancing performance.

What are the key skills and qualifications needed to thrive as a data collection associate, and why are they important?

To thrive as a Data Collection Associate, you need strong attention to detail, data entry skills, and familiarity with research or survey methodologies, often supported by a relevant degree or coursework. Proficiency with data collection tools, spreadsheets like Microsoft Excel, and sometimes survey platforms or database systems is typically required. Excellent organization, communication, and problem-solving skills help ensure accurate, timely data gathering and collaboration with team members. These skills and qualities are crucial for producing reliable datasets that support accurate analysis and informed decision-making.

What is a data collection associate?

Data Collection Associates are professionals responsible for gathering, recording, and verifying data for a variety of purposes such as research, analysis, or business operations. They may collect information through surveys, interviews, observations, or by compiling data from existing records. Their work ensures that organizations have accurate and reliable data to inform decision-making, strategy, and reporting. Data Collection Associates often work in sectors like healthcare, market research, education, and government.
What are the most commonly searched types of Data Collection jobs in Detroit, MI? The most popular types of Data Collection jobs in Detroit, MI are:
What are popular job titles related to Data Collection Associate jobs in Detroit, MI? For Data Collection Associate jobs in Detroit, MI, the most frequently searched job titles are:
What job categories do people searching Data Collection Associate jobs in Detroit, MI look for? The top searched job categories for Data Collection Associate jobs in Detroit, MI are:
Data Collection Associate jobs near you

Clinical Research Coordinator

Hypertension Nephrology Associates

Livonia, MI • On-site

Full-time

Medical, Dental, Retirement, PTO

Posted 28 days ago

Job description

Salary: $48,000 $60,000 annually


Position Overview

We are seeking a detail-oriented and patient-focused Clinical Research Coordinator to support our clinical research program. This role combines clinical care responsibilities with research coordination and administrative support.


The ideal candidate will bring experience in clinical trials, strong organizational skills, and a foundational understanding of study protocols and GCP guidelines. This role is well-suited for a Medical Assistant with research experience who is looking to further develop their skills in a clinical trials setting.


RESPONSIBILITIES

  • Assist in the coordination and execution of clinical trial activities in accordance with study protocols and ICH-GCP guidelines
  • Prepare study materials, equipment, and documentation for patient visits
  • Conduct protocol-specific procedures, interviews, and data collection
  • Maintain accurate and complete study documentation, including regulatory binders and source documents
  • Perform data entry and resolve study-related data queries
  • Verify patient records post-visit to ensure completeness and protocol compliance
  • Support subject recruitment, visit tracking, scheduling, and study-related financial tracking
  • Assist with the development and maintenance of source documents
  • Maintain organized and audit-ready study files (paper and electronic)
  • Provide administrative support across active clinical trials
  • Assist providers with patient care workflows during clinic visits
  • Collect patient medical histories and document clinical information
  • Perform vital signs, phlebotomy, and basic clinical procedures
  • Support medication reconciliation and communicate updates to providers
  • Maintain accurate documentation in the Electronic Medical Record (EMR) system
  • Educate patients on treatment plans, study participation, and follow-up care
  • Assist with scheduling, patient communication, and follow-up coordination
  • Ensure a clean, organized, and well-functioning clinical environment


QUALIFICATIONS

    • Previous administration experience in a private practice or clinical setting
    • IT Proficiency (Microsoft Office package)
    • Good verbal and written communication skills
    • Strong attention to detail and organizational skills
    • Proficiency with electronic medical records (EMR) and electronic data capture (EDC) systems
    • Clinical trials and/or medical practice experience
    • Experience managing essential documents for clinical trials according to ICH GCP
    • Experience using electronic data capture systems
    • Experience with phlebotomy, EKG, and Vital signs collection
    • Associate's degree in a science, technical, health-related field, or another applicable discipline (not required in lieu of experiences and certifications


BENEFITS

    • Completion of Good Clinical Practice (GCP) training
    • CME hours
    • 401(k)
    • Dental insurance
    • Health insurance
    • Paid time off


LOCAL CANDIDATES PREFERRED / NO RELOCATION ASSISTANCE