1

Study Com Jobs in Troy, MI (NOW HIRING)

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 ...

Mechanical Design Engineer

Plymouth, MI ยท 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 ...

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 ...

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 ...

Showing results 21-40

Study Com information

See Troy, MI salary details

$20.9K

$118.7K

$195.2K

How much do study com jobs pay per year?

As of Sep 4, 2026, the average yearly pay for study com in Troy, MI is $118,748.00, according to ZipRecruiter salary data. Most workers in this role earn between $80,600.00 and $148,800.00 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 cities near Troy, MI are hiring for Study Com jobs?

Cities near Troy, MI with the most Study Com job openings:

Infographic showing various Study Com job openings in Troy, MI as of August 2026, with employment types broken down into 1% As Needed, 73% Full Time, 21% Part Time, 1% Temporary, and 4% Contract. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution, with an average salary of $118,748 per year, or $57.1 per hour.

Clinical Research Coordinator

Actalent

Detroit, MI โ€ข Hybrid

$27 - $35/hr

Full-time, Contractor

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 16 days ago


Job description

Clinical Research Coordinator

About the Role

Join a leading cancer research team as a Clinical Research Coordinator supporting complex oncology clinical trials. In this patient-facing role, you will work directly with participants throughout the clinical trial process, including screening, consenting, scheduling, and conducting study visits. You will collaborate closely

with research nurses, investigators, and multidisciplinary teams while supporting multiple active studies within a thoracic or Phase I oncology

program.

Key Responsibilities

  • Coordinate and conduct patient visits in accordance with clinical trial protocols
  • Screen and recruit eligible study participants, including chart reviews and eligibility assessments
  • Obtain informed consent and educate patients on study requirements
  • Support participant enrollment, follow-up, and retention activities
  • Collaborate with research nurses and study teams to ensure protocol compliance
  • Maintain accurate study documentation and patient records
  • Assist with recruitment efforts through referrals, tumor boards, and new patient consults
  • Support approximately 10 study participants across multiple ongoing clinical trials

Required Qualifications

  • Bachelor's degree
  • Minimum 1 year of patient-facing clinical research experience
  • Experience consenting patients and conducting study visits
  • Experience working on clinical drug trials with moderate to high complexity
  • Strong clinical and patient interaction skills
  • Basic understanding of clinical research regulations and processes

Preferred Qualifications

  • Oncology clinical research experience
  • Phase I clinical trial experience
  • SOCRA or ACRP certification
  • Clinical research certification or willingness to obtain certification

Schedule & Work Environment

  • Full-time, 8-hour shifts
  • Start times between 7:00 AM and 9:00 AM based on patient schedules
  • Collaborative team consisting of Clinical Research Coordinators and Research Nurses
Job Type & Location

This is a Contract to Hire position based out of Detroit, MI.

Pay and Benefits

The pay range for this position is $27.00 - $35.00/hr.

Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type

This is a hybrid position in Detroit,MI.

Application Deadline

This position is anticipated to close on Sep 11, 2026.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications withoutregard to race, sex, age, color, religion, national origin, veteran status, disability,sexual orientation, gender identity, genetic information or any characteristic protectedby law.

If you would like to request a reasonable accommodation, such as the modification oradjustment of the job application process or interviewing process due to a disability,please email actalentaccommodation@actalentservices.com for other accommodation options.

San Francisco Fair Chance Ordinance:Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in thecity and county of San Francisco, we will consider for employment qualified applicantswith arrest and conviction records.

Massachusetts Lie Detector:It is unlawful in Massachusetts to require or administer a lie detector test as acondition of employment or continued employment. An employer who violates this lawshall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI):We may use Artificial Intelligence (AI) to support parts of our hiring process,including sourcing, screening, and evaluating candidates. AI helps assess applicationsand qualifications, but final decisions are made by our hiring team. By applying, youacknowledge and agree that your application may be reviewed using AI tools.


Actalent logo

About Actalent

Sourced by ZipRecruiter

Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. We're supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent promotes consultant care and engagement through experiences that enable continuous development. Our people are the difference. Actalent is an operating company of Allegis Group, the global leader in talent solutions.

Industry

Business management consulting

Company size

5,001 - 10,000 Employees

Headquarters location

Hanover, MD, US

Social media