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Study Com Jobs in Michigan (NOW HIRING)

MMS

Senior Biostatistician - Remote (US)

Canton, MI · On-site

Visit www.mmsholdings.com or follow MMS on LinkedIn. Senior Biostatistician: Responsibilities ... Create SAP TLFs shells for all phases and studies. * Review ADAM and TLFs; work with client and ...

Schaeffler Group

CNC Machinist Apprentice

MI · On-site

$17 - $22/hr

We look forward to your application. www.schaeffler.com/careers Your Contact Schaeffler Group USA Inc. Keywords: Students; Apprenticeship/Dual studies; Full-Time; Not Applicable; Administration ...

Schaeffler

CNC Machinist Apprentice

Armada, MI · On-site

$19.75 - $27/hr

We look forward to your application. www.schaeffler.com/careers Your Contact Schaeffler Group USA Inc. Keywords: Students; Apprenticeship/Dual studies; Full-Time; Not Applicable; Administration ...

Schaeffler

CNC Machinist Apprentice

Armada, MI

$19.75 - $27/hr

We look forward to your application. www.schaeffler.com/careers Your Contact Schaeffler Group USA Inc. Keywords: Students; Apprenticeship/Dual studies; Full-Time; Not Applicable; Administration ...

MMS

Principal Biostatistician - Remote

Canton, MI · On-site

Visit www.mmsholdings.com or follow MMS on LinkedIn. Roles and Responsibilities * Lead complex ... Provide valuable feedback to the Sponsor on the statistical aspects of the study. * Prepare and ...

Covista

Maternal Child Clinical Faculty (Part-Time)

Troy, MI · On-site

$37.25 - $50.75/hr

... Studies, Public Health Certificate programs, and a Master of Social Work degree. Learn more about Chamberlain University, part of Covista, at www.covista.com There is one very significant way ...

MMS

Nonclinical Writer

Canton, MI · On-site

Visit www.mmsholdings.com or follow MMS on LinkedIn. This person will participate in the ... Ability to develop a mapping plan for the placement of nonclinical studies within structure of ...

MMS Holdings Inc.

Nonclinical Writer

Canton, MI · On-site

Visit www.mmsholdings.com or follow MMS on LinkedIn. This person will participate in the ... Ability to develop a mapping plan for the placement of nonclinical studies within structure of ...

SFV Services

Be Seen First

Construction Estimator

Southfield, MI · On-site

$75K - $85K/yr

Prepare estimates and budgets for construction by studying plans and specifications. * Familliar ... com

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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 Jun 9, 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 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 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 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 Study Com jobs?

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 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 June 2026, with employment types broken down into 2% As Needed, 83% Full Time, 8% Part Time, 2% Temporary, 4% Contract, and 1% Nights. Highlights an 94% Physical, 3% Hybrid, and 3% Remote job distribution, with an average salary of $109,202 per year, or $52.5 per hour.
Senior Biostatistician - Remote (US)

Senior Biostatistician - Remote (US)

MMS Holdings Inc.

Canton, MI • On-site, Remote

Full-time

Posted 28 days ago

Job description

About MMS
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.
Senior Biostatistician:
Responsibilities:
  • Create randomization and kit schedules independently, collaborate with sponsor, randomization and drug supply management teams.
  • Develop phase 1-4 SAPs and make significant contributions to iSAPs. Create SAP TLFs shells for all phases and studies.
  • Review ADAM and TLFs; work with client and programmers to resolve comments.
  • Strong programming and logic skills (working knowledge of SAS)
  • Ability to apply drug development knowledge during production of high quality statistical analyses.
  • Perform sample size calculations for a variety of scenarios and study designs.
  • Leads projects (all phases and even a program of studies) and smaller submissions, manages client meetings, CRMs, collaborates well with regulatory, PMs and sponsor.
  • Strong knowledge of CDISC (especially SDTM and ADaM), looks to understand guidance from FDA from the different therapeutical areas.
  • Understand the various tools that we work with
  • High level knowledge of drug development as it pertains to biostatistics.
  • Provides support to Data Safety Monitoring Boards (DSMB) by preparing and presenting output as the unblinded statistician.
  • Review the statistical section of a Sponsor's protocol and ensure that the appropriate statistical methods are proposed for the study design and objectives. Provide valuable feedback to the Sponsor on the statistical aspects of the study. Create the statistical section of the Sponsor's protocol with minimal support
  • High proficiency with MS Office applications
  • Demonstrate an understanding of project management-related tasks such as timelines, scope and resource requirement estimation.
  • Provide ICH guideline based input as applicable to statistics.
  • Prepare and review statistical methods and results sections for the CSR with minimal support in collaboration with in-house medical writers.
Requirements:
  • College graduate in Biostatistics, Statistics, or Mathematics discipline or related field, masters or PhD preferred, or many years of related experience required.
  • Minimum of 5 years' experience in Biostatistics or similar field required.
  • Expert knowledge of scientific principles and concepts.
  • Has high level knowledge of drug development as it pertains to biostatistics; has the ability to apply drug development knowledge during production of high quality statistical analyses.
  • Strong SAS programming, SAS base, SAS macro experience.
  • Thorough knowledge and understanding of clinical data preferred.
  • Strong experience with data and production of TLGs.
  • Excellent scientific writing skills.
  • Strong resource for biostatistics; willing to guide others in a variety of biostatistical techniques.
  • Proficiency with MS Office applications.
  • Hands-on experience with clinical trial and pharmaceutical development preferred.
  • Good communication skills and willingness to work with others to clearly understand needs and solve problems.
  • Excellent problem-solving skills.
  • Good organizational and communication skills.
  • Familiarity with 21 CFR Part 11, FDA, and GCP requirements.
  • Basic understanding of CROs and scientific & clinical data/terminology, & the drug development process.

Please consider your application unsuccessful if we do not reach out to you within 14 days of your submission.

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