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Data Entry Coding Jobs in Michigan (NOW HIRING)

... 5. Data entry that supports office needs, ICD-10 and CPT coding, and outreach registrations. 6. Transcribe dictation reports, and clerical duties, that supports pathologists. Required: • High ...

Billing Specialist

Plymouth, MI · On-site

$18.25 - $24.75/hr

... coding) * Strong data entry skills (both speed and accuracy) * Highly organized and excellent at time management * Effective Communicator both externally with providers and with internal team

... data entry, customer service, and recordkeeping; or Associates Degree in Medical Insurance Billing and Coding or related field that includes courses in medical insurance billing and/or coding.

... data entry, customer service, and recordkeeping; or Associates Degree in Medical Insurance Billing and Coding or related field that includes courses in medical insurance billing and/or coding. • ...

... data entry, customer service, and recordkeeping; or Associates Degree in Medical Insurance Billing and Coding or related field that includes courses in medical insurance billing and/or coding. • ...

Detail-oriented with a strong focus on accuracy in data entry, eligibility verification, pharmacy calculations, and HCPCS coding to support clean claims and timely reimbursement. * Strong customer ...

Showing results 41-60

Data Entry Coding information

See Michigan salary details

$9

$16

$24

How much do data entry coding jobs pay per hour?

As of Aug 19, 2026, the average hourly pay for data entry coding in Michigan is $16.97, according to ZipRecruiter salary data. Most workers in this role earn between $14.23 and $19.09 per hour, depending on experience, location, and employer.

What is a data entry coding?

A Data Entry Coding job involves entering, organizing, and processing data into a digital database or system, often using specific codes or classifications. This role is common in industries like healthcare, finance, and logistics, where accurate data categorization is essential. Employees ensure data integrity, follow company guidelines, and may work with specialized software. Attention to detail, typing speed, and accuracy are key skills for success in this role.

What are the main daily tasks and challenges for someone working in data entry coding?

Daily responsibilities in Data Entry Coding typically include inputting large volumes of information into databases, verifying the accuracy of data, and ensuring that codes or classifications are applied correctly. One common challenge is maintaining a high level of accuracy and speed while managing repetitive tasks, which requires strong attention to detail and concentration. Team members may also collaborate with supervisors or quality control staff to resolve discrepancies or clarify coding guidelines. Consistent communication and the ability to quickly adapt to updated processes or software systems are also important aspects of the role.

What are the key skills and qualifications needed to thrive in data entry coding, and why are they important?

To excel as a Data Entry Coding professional, you need fast and accurate typing skills, attention to detail, and a solid understanding of data management practices, often with a high school diploma or equivalent. Familiarity with data entry software, databases, spreadsheet applications, and sometimes industry-specific coding systems such as ICD-10 for medical data is valuable. Outstanding organizational skills, reliability, and the ability to maintain focus during repetitive tasks set top performers apart. These competencies are crucial for ensuring data accuracy, meeting deadlines, and supporting seamless workflow within organizations.

What are the most commonly searched types of Data Entry Coding jobs in Michigan?

The most popular types of Data Entry Coding jobs in Michigan are:

What are popular job titles related to Data Entry Coding jobs in Michigan?

For Data Entry Coding jobs in Michigan, the most frequently searched job titles are:

Infographic showing various Data Entry Coding job openings in Michigan as of August 2026, with employment types broken down into 75% Full Time, and 25% Part Time. Highlights an 90% In-person, and 10% Hybrid job distribution, with an average salary of $35,303 per year, or $17 per hour.

Senior Clinical Data Manager (Remote - US)

MMS

Canton, MI • On-site

Full-time

Posted 2 days ago

New


Job description

Are you looking to join a company where your contributions truly matter, and where you'll be part of a supportive, innovative team? MMS is a award-winning, data-focused clinical research organization (CRO). We pride ourselves on being a Great Place to Work certified organization, recognized for our exceptional culture and industry best employee retention rate. We support the pharmaceutical, biotech, and medical device industries with our proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS not only maintains an industry-leading customer satisfaction rating but also fosters a collaborative and inclusive work environment where employees can thrive. Join us at MMS and be part of a team that is shaping the future of clinical research.
 
Discover more about our exciting opportunities and why MMS is a great place to advance your career. Visit www.mmsholdings.com or follow MMS on LinkedIn.
Roles and Responsibilities:
  • Confidently displays excellent internal and external customer service.
  • Has proficiency and knowledge of multiple EDC systems; applies this knowledge to advise customers regarding the best-fit EDC solution.
  • Interacts directly and independently with DM suppliers including EDC and/ or IWR; expert communicator, where necessary negotiating with supplier to meet business needs.
  • Interacts directly and independently with client to coordinate all facets of projects; expert communicator; builds and maintains strong client contacts and relationships.
  • Responsible for entire data management process from study set-up to study close-out; primary contact on all data management study-specific issues; has high-level knowledge of drug development as it pertains to data management.
  • Actively participates in protocol review with clients, providing suggestions regarding ability to capture protocol information in database successfully.
  • Strong understanding of GCP/ ICH guidelines and FDA regulations, as applicable to data management.
  • Creates training exercises; serves as mentor and trains new clinical data managers.
  • Provides oversight and resolves all issues in data management study processing activities including CRF tracking and data entry, integration of external electronic data (e.g., lab data) with clinical database, data validation and review, query processing and resolution, adverse event and medication coding, SAE reconciliation, database lock and database QC audits.
  • Oversees and develops data management study documentation including Case Report Forms, CRF Completion Guidelines, Database Design via annotated CRFs, Validation specifications (edit checks), and Data Management Plan.
  • Preparation of any study tracking and metric reports for use by the study team.
  • Oversees execution of user acceptance testing (UAT) of study-specific systems and applications.
  • Interacts with cross-functional team members to ensure completion of all timelines and studies.
  • Participates in data management and/or organizational initiatives.
  • Initiates SOP updates and provide specifications for DM systems/ tools and process enhancements.
  • May act as resource for QC activities in collaboration with QC Coordinator.
  • Understands and follows processes related to project management as appropriate for data management projects (e.g., updating PSS, close-out procedures, etc.).
  • Confident, positive attitude displayed towards clients and projects.
  • Willingness to learn new skills and expand knowledge of drug development.
  • Leads data management projects with little management oversight.
  • Ability to work independently and resolve issues.
  • Ability to clearly articulate the DM services offered at company, including pros and cons of various DM approaches (specific to a client or operating model). To include potential attendance at (web or remote) capabilities and bid defense meetings.
Requirements:
  • Bachelor’s or Master’s Degree in scientific or health care field preferred with industry or relevant experience.
  • 5+ years’ experience in data management field with a minimum of 1 year of experience leading projects.
  • Extensive knowledge of paper CRF study systems, EDC, and hybrid CDM systems.
  • Extensive knowledge of Clinical Operations SOPs and Working Practices.
  • Excellent verbal and written communication skills, as well as, interpersonal and organizational skills.

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M. M. S. logo

About M. M. S.

Sourced by ZipRecruiter

Industry

Pharmaceutical and medicine manufacturing

Company size

1 - 10 Employees

Headquarters location

Los Angeles, CA, US

Year founded

1980