ZipRecruiter

Log In

1

Study Com Jobs in Plainfield, IL (NOW HIRING)

GovernmentJobs.com

Executive Secretary 24-E-16

Chicago, IL · On-site

$55K - $85K/yr

As secretary to a Division Chief, the Executive Secretary shall conduct special projects and studies by gathering data, coordinating, monitoring and completing assigned projects. Additionally this ...

next page

Showing results 1-20

All JobsStudy Com JobsStudy Com Jobs in Plainfield, IL

Study Com information

See Plainfield, IL salary details

$21.4K

$122.1K

$200.8K

How much do study com jobs pay per year?

As of Sep 7, 2026, the average yearly pay for study com in Plainfield, IL is $122,121.00, according to ZipRecruiter salary data. Most workers in this role earn between $82,800.00 and $153,000.00 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 Plainfield, IL?

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

What cities near Plainfield, IL are hiring for Study Com jobs?

Cities near Plainfield, IL with the most Study Com job openings:

Study Com jobs near you
Infographic showing various Study Com job openings in Plainfield, IL as of August 2026, with employment types broken down into 1% As Needed, 74% Full Time, 20% Part Time, and 5% Contract. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution, with an average salary of $122,121 per year, or $58.7 per hour.

Study Coordinator

Hematogenix Laboratory Sv

Tinley Park, IL • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 5 days ago

Job description

 
 
 About Hematogenix 

Want a job with greater meaning and higher purpose? Every day Hematogenix employees are warriors fighting a noble and global war on cancer. Helping patients every day, and helping partners every day – with our diagnostic and research services. 

Hematogenix is looking for talented and highly motivated individuals to join our team. We offer a competitive benefit package and career development opportunities to help you achieve your highest professional and personal goals. We are eager to show you all we have to offer and how you can grow with us.

Hematogenix is a specialized contract research organization and clinical laboratory with a global presence. Our team of board-certified clinical, anatomic and research pathologists work in conjunction with top scientists from around the world to provide quality testing, consultation, and guidance for all aspects of the company’s pharma and diagnostic services. 


 Job Purpose:

The Clinical Study Coordinator supports the successful delivery of clinical trial projects via operational/day-to-day management of workflows. Deliver excellent customer service to project stakeholders (e.g., clients, clinical sites). 

*Please note that this position requires you to be onsite at our Illinois, USA location.


 Accountabilities/Work Activities:

Study Initiation

  • Possess strong working knowledge of company capability’s and how it typically aligns with clients’ objectives and timelines.
  • Comfortable developing and maintaining relationships with various project stakeholders where needed (external and internal)

Planning & Design

  • Contribute, when necessary, operational insights that will impact project scope.
  • Assist the Project Managers with creation of study specific laboratory binders and regulatory documents.

Executing

  • Attend in-house initiation meetings with all project personnel in order to understand individual contributions of all, as well as overall study objectives and timelines.
  • Provide guidance to Pharma Accessioning Team regarding query generation.
  • Create and send clearly written data clarification messages to ensure outstanding queries are resolved in a timely fashion according to Communication and Escalation Plan established with each Sponsor.
  • Maintain study tracking spreadsheets/documents in real time if applicable.
  • Communicate effectively (verbal and written) when interacting with external stakeholders (e.g., CRAs, SCs, PIs, etc.)
  • Interact effectively with all in-house project personnel and provide clear communication on status of cases (query resolution) or specific requests (e.g., expedited testing requests
  • Perform data entry if needed and/or manage data entry needs of projects to ensure daily/weekly completion occurs.
  • Process sample repatriations and maintain associated documentation.

Monitoring & Controlling

  • Participate in regular internal meetings with Project Manager to feed in views of project personnel, outline operational challenges, and learn of wider project progress.
  • Participate in regular conference calls with clients.
  • Provide support to Project Manager during client monitoring visits.
  • Ensure project supplies and day-to-day resources are always appropriately used in an effort to reduce waste and increase efficiency.

Study Closing

  • Contribute to internal project closing meetings in order to share best practice.
  • Provide QC support to Project Manager during close out visits.


 Experience and Education

  • Bachelor of Science degree or similar degree related to the role 
  • 1-2 years’ experience in Clinical Laboratory Science 


 Skills and Qualifications

  • Knowledge of GCP/CAP/CLIA and global clinical research industry
  • Must be able to communicate effectively and persuasively, both verbally and in writing, with all levels of in-house Hematogenix personnel and other project stakeholders (e.g., CRAs, site officials)
  • Working experience with laboratory information systems
  • Personal computer skills (Microsoft Word, Excel, Power Point, etc.)
  • Ability to ambulate throughout the office and laboratory.

Benefits we Offer:

  • Medical
  • Dental 
  • Vison 
  • Life
  • 401k 
  • PTO
  • Competitive Salary

Contact Information:

 jobs@hematogenix.com; www.hematogenix.com


Hematogenix provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.

This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.