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Remote Clinical Data Entry Jobs in Michigan (NOW HIRING)

Danaher

Principal Clinical Scientist

Detroit, MI · On-site +1

... remote based (can also be onsite in Chaska, MN). At Danaher Diagnostics, our vision is to be the ... Ability to critically review and interpret scientific and clinical trial data, and oversee the ...

Zwicker & Associates, P.C.

Document Clerk

Troy, MI · On-site +1

$17/hr

This position is remote after the first day. Candidates must have a reliable home workspace and the ... Data entry and/or administrative experience a plus * Strong attention to detail and problem-solving ...

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Remote Clinical Data Entry information

What is a remote clinical data entry?

A Remote Clinical Data Entry job involves inputting, managing, and updating clinical data in digital systems from a remote location. Professionals in this role ensure accuracy, confidentiality, and compliance with healthcare regulations. They may work with clinical trial data, patient records, or other medical information. Strong attention to detail, familiarity with medical terminology, and proficiency in data entry software are essential for success in this field.

What are the key skills and qualifications needed for remote clinical data entry?

To excel in Remote Clinical Data Entry, you need strong attention to detail, fast and accurate typing skills, and a familiarity with medical terminology, often supported by a diploma or coursework in health sciences or medical administration. Knowledge of clinical data management systems (such as EDC platforms), electronic health records (EHRs), and basic proficiency with spreadsheet software like Excel is typically required, and certification in data entry or health information management can be advantageous. Exceptional organizational skills, reliability, and the ability to work independently while maintaining clear communication with remote teams are standout soft skills for this role. These abilities ensure accurate, timely data handling, facilitate compliance with healthcare regulations, and contribute to the integrity of patient records and research data.

What does a typical workday look like for remote clinical data entry?

A typical workday in a remote clinical data entry position involves reviewing clinical documents and inputting critical data into electronic databases or health record systems. You will regularly communicate with healthcare professionals, study coordinators, or data managers to clarify details and ensure data accuracy. Most days require a balance between independent data entry tasks and virtual team meetings or status updates, all within strict privacy and compliance guidelines. The remote environment offers flexibility, but it also requires excellent self-management to meet deadlines and maintain high accuracy standards. Over time, this experience can open doors to roles in clinical data management, trial coordination, or health information analysis.

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

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

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

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

What job categories do people searching Remote Clinical Data Entry jobs in Michigan look for?

The top searched job categories for Remote Clinical Data Entry jobs in Michigan are:

What cities in Michigan are hiring for Remote Clinical Data Entry jobs?

Cities in Michigan with the most Remote Clinical Data Entry job openings:

Remote Clinical Data Entry jobs near you
Infographic showing various Remote Clinical Data Entry job openings in Michigan as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 12% Part Time, 4% Contract, and 1% Nights. Highlights an 86% Physical, 3% Hybrid, and 11% Remote job distribution.

Study Design Statistician (Remote)

MMS Holdings Inc.

Canton, MI • On-site, Remote

Full-time

Re-posted 24 days ago

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.
As part of our Strategic Statistical Services Arm, this is a full-time role with emphasis on being an internal and external SME for clinical trial design, together with providing consultation to advise clients on a range of broader statistical issues, and will have an internal job title of Strategic Statistician.
Job Description:
Our experienced statisticians and programmers develop intellectual property and assets to support the design and analysis of clinical trials, precision medicine and real-world data analytics. We address the emerging analytics needs of the Industry with our biostatistics services, bespoke algorithms and unique, state of the art, proprietary, cloud-based trial simulation software KerusCloud. Working alongside innovative statisticians you will be responsible for leading the full life-cycle of KerusCloud support and statistical services, from:
  • Assisting customers with their study design with a particular focus on simulation with KerusCloud to ensure they are aligned with the study objectives.
  • Preparation of study protocols and development of Statistical Analysis Plans and Statistical Analysis Reports.
  • Summarize, analyze and visualize study data using a variety of statistical methods, ultimately delivering results to an agreed timeline with optimal quality.
  • Provide statistical consultancy support to sponsors across the full span of clinical development, including oversight of third-party statistical and programming deliverables.
  • Maintain current knowledge of relevant research techniques such as modelling, simulation and experimental design and participate in continuous professional development activity.
  • Support pre-sales discussions to understand and identify client needs, then contribute to technical solutions and resource/ cost estimates.
  • Collaborate with the Product Development team defining key features and statistical aspects of KerusCloud.
  • Provide input and support to Marketing of KerusCloud, including demonstrations to clients, white papers, etc.

Requirements:
  • Bachelors degree in mathematics, statistics, physics, pharmacology or with a strong statistical component, Masters or PhD preferred.
  • 5-7 years of experience in the application of medical statistics (pharma, CRO, academic).
  • Willingness to engage with clients to understand and research problems and provide creative, business-orientated solutions.
  • Experience in delivering customer projects to high quality standards.
  • Experience in SAS and/ or R statistical software packages.
  • Experience in study design and protocol and report-writing preferred.
  • Experience of modelling and simulation techniques to explore complex study designs preferred.
  • Experience of Bayesian approaches to design and analysis of clinical data preferred.
  • Experience of early-phase drug development processes including innovative/ adaptive study design preferred.

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