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Clinical Data Associate Jobs in Three Rivers, MI

Eurofins Scientific

Associate Scientist

Portage, MI · On-site

It also has a rapidly developing presence in highly specialized and molecular clinical diagnostic ... Processes data, generates reports, and evaluates data * Trains others in laboratory procedures

New

Eurofins

Associate Scientist

Portage, MI · On-site

It also has a rapidly developing presence in highly specialized and molecular clinical diagnostic ... Processes data, generates reports, and evaluates data * Trains others in laboratory procedures

New

Abaxis

Technical Associate

Portage, MI · On-site

This role assists in all phases of clinical and preclinical studies, associated with the discovery ... data collection in accordance with regulatory requirements. * Performs a variety of animal ...

- Zoetis Belgium S.A.

Technical Associate

Portage, MI · On-site

This role assists in all phases of clinical and preclinical studies, associated with the discovery ... data collection in accordance with regulatory requirements. * Performs a variety of animal ...

Beacon Medical Group Elkhart East

NP - Trauma

Elkhart, IN · On-site

$105K - $136K/yr

Provides clinical and administrative assistance to BMG programs, etc. Works collaboratively in the ... Interpreting and integrating data to determine appropriate diagnostic and therapeutic procedures as ...

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All JobsClinical Data Associate JobsClinical Data Associate Jobs in Three Rivers, MI

Clinical Data Associate information

See Three Rivers, MI salary details

$12

$35

$80

How much do clinical data associate jobs pay per hour?

As of Sep 13, 2026, the average hourly pay for clinical data associate in Three Rivers, MI is $35.92, according to ZipRecruiter salary data. Most workers in this role earn between $27.07 and $35.91 per hour, depending on experience, location, and employer.

What does a clinical data associate do?

A Clinical Data Associate is responsible for collecting, validating, and managing clinical trial data to ensure its accuracy, completeness, and compliance with regulatory standards. They work closely with clinical research teams to monitor data quality, resolve discrepancies, and prepare data for analysis. Their work is essential in supporting drug development and regulatory submissions by ensuring reliable and high-quality clinical data.

What does a clinical data associate do?

A clinical data associate is responsible for tracking data and results in a research study. As a clinical data associate, your job duties are to collect data, perform data management, and input data into any software used by your team. You work on a research team, so you must be able to work collaboratively and have excellent organizational skills. While you spend most of your time in an office, you may be required to work in the field to record data. The only universal qualifications needed for this career are a background in health care or medical science research and experience with data management software like Oracle Clinical, Microsoft Excel, and SPSS.

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

To thrive as a Clinical Data Associate, you need a solid understanding of clinical research, data management principles, and attention to detail, often supported by a degree in life sciences or a related field. Familiarity with clinical data management systems (CDMS), electronic data capture (EDC) tools, and knowledge of regulatory guidelines like GCP or CDISC is typically required. Strong organizational skills, analytical thinking, and clear communication set outstanding candidates apart in this role. These skills ensure the accuracy, integrity, and compliance of clinical trial data, which are crucial for successful research outcomes and regulatory approval.

What are some common challenges faced by clinical data associates when ensuring data quality during clinical trials?

Clinical Data Associates often encounter challenges such as identifying and resolving discrepancies in large datasets, maintaining strict compliance with regulatory standards, and coordinating timely data entry from multiple sites. They must work closely with clinical research teams and data managers to clarify ambiguous data and implement data cleaning procedures. Staying organized and detail-oriented is essential to ensure data accuracy and the successful progression of clinical trials.

What is the difference between Clinical Data Associate vs Clinical Research Coordinator?

AspectClinical Data AssociateClinical Research Coordinator
Primary RoleManage and ensure accuracy of clinical trial dataOversee trial operations, patient recruitment, and site management
CredentialsBachelor's in life sciences or related field; familiarity with data managementBachelor's in health sciences or related field; clinical trial experience
Work EnvironmentData management teams, clinical trial databasesClinical sites, hospitals, research facilities
Industry UsagePharmaceutical companies, CROs, biotech firmsHospitals, research institutions, clinical trial sites

While both roles support clinical trials, a Clinical Data Associate primarily focuses on managing and validating trial data, ensuring accuracy and compliance. In contrast, a Clinical Research Coordinator handles the overall trial operations, including patient recruitment and site coordination. Both roles require relevant certifications and work within the clinical research industry, but their daily responsibilities differ significantly.

More about Clinical Data Associate jobs

What cities near Three Rivers, MI are hiring for Clinical Data Associate jobs?

Cities near Three Rivers, MI with the most Clinical Data Associate job openings:

Clinical Data Associate jobs near you
Infographic showing various Clinical Data Associate job openings in Three Rivers, MI as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 15% Part Time, 1% Temporary, and 2% Contract. Highlights an 85% Physical, 4% Hybrid, and 11% Remote job distribution, with an average salary of $74,722 per year, or $35.9 per hour.

Associate Scientist

Portage, MI • On-site

Eurofins Scientific
Scientific Research and Development Services • 10K+ employees
Learn more about Eurofins Scientificexternal

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted yesterday

New

Eurofins rating

7.5

Company rating: 7.5 out of 10

Based on 181 frontline employees who took The Breakroom Quiz

Job description

Company Description

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.

The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organization services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organizations. It also has a rapidly developing presence in highly specialized and molecular clinical diagnostic testing and in-vitro diagnostic products.

In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralized and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.

2025, Eurofins generated total revenues of EUR 7.296 billion, and has been among the best performing stocks in Europe over the past 20 years.

Job Description
  • Performing physical, chemical, and instrumental analysis of active pharmaceutical ingredients and finished pharmaceutical products (tablets, capsules, parenterals, devices, liquids, creams, and gels) and animal health products
  • Preparing standards and samples for analysis; running the instrumentation independently including, but not limited to, various chromatographic systems, Karl Fischer (Coulometric and Volumetric), UV/Spec, HPLC, and dissolution apparatus
  • Executing method transfer protocols
  • Performing monthly maintenance of laboratory equipment
  • Working efficiently, documenting work clearly, and performing tests accurately
  • Ensuring that the client receives quality data by reviewing laboratory data for accuracy, clarity, and adherence to GMP and/or GLP regulations
  • Reads and understands analytical procedures (compendial and client supplied) and internal SOPs
  • Processes data, generates reports, and evaluates data
  • Trains others in laboratory procedures
  • Performs laboratory maintenance
  • Communicates with vendors and repair personnel
  • Writes investigations
  • Leads project/test areas and perform method transfers/feasibility studies
  • Preparing standards and samples for analysis; running the instrumentation independently including, but not limited to, various chromatographic systems, Karl Fischer (Coulometric and Volumetric), UV/Spec, HPLC, and dissolution apparatus
Qualifications

Minimum Qualifications:

  • Bachelor's degree in biology, chemistry, or other related degree concentration
  • Authorization to work in the United States indefinitely without restriction or sponsorship
Additional Information

Position is full-time, Tuesday to Friday, 8 a.m.-6 p.m. 4x10 schedule, with overtime as needed. Candidates currently living within a commutable distance of Portage, MI are encouraged to apply.

Excellent full time benefits including

  • Comprehensive medical coverage, dental, and vision options
  • Life and disability insurance
  • 401(k) with company match
  • Paid vacation and holidays

Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.

What Eurofins employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom

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About Eurofins

Sourced by ZipRecruiter

Industry

Scientific research and development services, biotechnology research and development and environmental consulting services

Company size

10,000+ Employees

Headquarters location

Leacock, PA, US

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