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Study Com Jobs in Michigan (NOW HIRING)

Actalent

Clinical Research Coordinator

Detroit, MI · Hybrid

$27 - $35/hr

Screen and recruit eligible study participants, including chart reviews and eligibility assessments ... com for other accommodation options. San Francisco Fair Chance Ordinance: Pursuant to the San ...

Actalent

Clinical Research Coordinator

Detroit, MI · Hybrid

$27 - $35/hr

Screen and recruit eligible study participants, including chart reviews and eligibility assessments ... com for other accommodation options. San Francisco Fair Chance Ordinance: Pursuant to the San ...

Collabera

Mechanical Design Engineer

Plymouth, MI · On-site

$72K - $98K/yr

Visit www.collabera.com to learn more about our latest job openings. Awards and Recognition ... Manage turbocharger assembly and BOM in the CAD. Create design layouts with stack up studies to ...

Johnson & Johnson Innovative Medicine

... com As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us ... As Study Director: * Is accountable and responsible for Study Protocol and Animal Use Protocol ...

Danaher

Principal Clinical Scientist

Detroit, MI · On-site +1

You will drive strategic study designs, ensuring regulatory compliance, and achieving key ... Check out our benefits at danaherbenefitsinfo.com. This job is also eligible for bonus/incentive ...

MMS

Senior Medical Writer (Remote)

Canton, MI · On-site

For more information, visit www.mmsholdings.com or follow MMS on LinkedIn. Responsibilities * Under ... Substantial clinical study protocol experience, as lead author, required * Experience leading and ...

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Showing results 41-60

All JobsStudy Com JobsStudy Com Jobs in Michigan

Study Com information

See Michigan salary details

$19.2K

$109.2K

$179.5K

How much do study com jobs pay per year?

As of Sep 5, 2026, the average yearly pay for study com in Michigan is $109,202.00, according to ZipRecruiter salary data. Most workers in this role earn between $74,100.00 and $136,800.00 per year, depending on experience, location, and employer.

What is a study com?

Study.com jobs refer to employment opportunities with Study.com, an online education platform that provides video lessons, study guides, and other educational resources. Job roles at Study.com can include content writers, curriculum developers, video editors, software engineers, and customer support specialists. Employees work to create and maintain high-quality educational content and ensure a positive learning experience for users. Some positions are remote or freelance, offering flexible work options. Working at Study.com can be a good fit for those passionate about education and technology.

What are the typical responsibilities of a study coordinator in a clinical research setting?

A Study Coordinator, often referred to as a Clinical Research Coordinator, is responsible for managing daily operations of clinical trials. This includes recruiting and screening study participants, obtaining informed consent, scheduling and conducting study visits, collecting and recording data, and ensuring compliance with regulatory requirements. Coordinators also act as a liaison between investigators, sponsors, and study participants, making strong organizational and communication skills essential. The role offers opportunities to learn about various aspects of clinical research, paving the way for career advancement into project management or regulatory affairs.

What are the key skills and qualifications needed to thrive as a study coordinator, and why are they important?

To thrive as a Study Coordinator, you need a solid understanding of clinical research protocols, regulatory compliance, and project management, often supported by a degree in life sciences or healthcare. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and certification such as CCRC or CCRP is typically required. Strong organizational skills, attention to detail, and effective communication are crucial soft skills for coordinating between study teams, participants, and regulatory bodies. These competencies ensure studies are conducted ethically, efficiently, and in accordance with regulatory standards, which is vital for research integrity and successful trial outcomes.

What is the difference between Study Com vs Study Coordinator?

AspectStudy ComStudy Coordinator
Required CredentialsTypically a bachelor's degree, sometimes certifications in clinical researchUsually a bachelor's degree, often with certifications like CCRP or CCRC
Work EnvironmentOffice-based, research institutions, hospitalsClinical settings, hospitals, research sites
Employer & Industry UsageResearch organizations, pharmaceutical companies, academic institutionsHospitals, clinics, research sites
Common Search & ComparisonOften compared for roles in clinical research teamsFrequently compared with Study Com as a supporting role

Study Coordinators and Study Com roles both support clinical research but differ mainly in scope and responsibilities. Study Coordinators typically handle day-to-day trial management, patient coordination, and data collection, while Study Com may focus on broader communication and administrative tasks within research projects. Both roles require relevant certifications and work in similar environments, making them closely related in the clinical research industry.

What are popular job titles related to Study Com jobs in Michigan?

For Study Com jobs in Michigan, the most frequently searched job titles are:

What job categories do people searching Study Com jobs in Michigan look for?

The top searched job categories for Study Com jobs in Michigan are:

What cities in Michigan are hiring for Study Com jobs?

Cities in Michigan with the most Study Com job openings:

Study Com jobs near you
Infographic showing various Study Com job openings in Michigan as of August 2026, with employment types broken down into 1% As Needed, 71% Full Time, 24% Part Time, and 4% Contract. Highlights an 93% Physical, 3% Hybrid, and 4% Remote job distribution, with an average salary of $109,202 per year, or $52.5 per hour.

CMM Programmer & Operator

ULTRAFORM INDUSTRIES, INC.

Romeo, MI • On-site

Other

Posted 5 days ago

Job description

Ultraform Industries is expanding our Quality team! We are officially on the hunt for a CMM Programmer/Operator with 3–5 years of automotive manufacturing experience.

If you are highly proficient in PC-DMIS, master of GD&T, and have a track record of flawless PPAP submissions and gage calibration management, we have a desk (and a CMM machine) with your name on it!

Job Responsibilities:

  • Performs layouts and documents results for PPAP submissions
  • Performs layouts for production process and compiles/evaluates gathered data to determine/maintain quality and reliability of products
  • Performs capability studies and R & R studies.
  • Layout inspection gages/fixtures, as needed. Ensure all calibrations are completed on or before their due dates. Minor gage repairs.
  • Support engineering by measuring tooling / some reverse engineering required.
  • Interprets engineering drawings, schematic diagrams or formulas and confers with management or engineering within limits of equipment capability
  • Reviews all print feasibilities for dimensioning and GD&T
  • Prepares graphs or charts of data, or enters data into computer for analysis
  • Helps with Audits, first pieces, receiving, training, etc. as needed
  • Completes hourly SPC measurements on production parts as required.

EDUCATION and/or EXPERIENCE:

CMM Programmer Experience 3-5 years

Automotive experience

Experience with PC DMIS software

Experience within a manufacturing environment providing metrology solutions

Strong GD&T and Quality Systems knowledge

Knowledgeable in surface plate layouts

Proficient with Windows OS


Looking to apply? Send in your resume to Careers@ultraformindustries.com or give us a call at 1(586)752-4508.

Apply