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Study Com Jobs in Evanston, IL (NOW HIRING)

MMS

Study Design Statistician (US)

Chicago, IL · On-site

Visit www.mmsholdings.com or follow MMS on LinkedIn. As part of our Strategic Statistical Services ... Preparation of study protocols and development of Statistical Analysis Plans and Statistical ...

AbbVie

Senior Clinical Pharmacologist

North Chicago, IL · On-site

$109K/yr

For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn ... Contribute to clinical development by supporting Phase 1-4 studies including study design, and ...

Walgreens

Senior Reporting Analyst

Deerfield, IL · On-site

$71K - $114K/yr

Job Summary This role involves leading an analytics team which studies a variety of contact center ... About Walgreens Founded in 1901, Walgreens (www.walgreens.com) proudly serves nearly 9 million ...

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Showing results 1-20

All JobsStudy Com JobsStudy Com Jobs in Evanston, IL

Study Com information

See Evanston, IL salary details

$21.1K

$120.2K

$197.7K

How much do study com jobs pay per year?

As of Aug 3, 2026, the average yearly pay for study com in Evanston, IL is $120,236.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,600.00 and $150,700.00 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 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 popular job titles related to Study Com jobs in Evanston, IL? For Study Com jobs in Evanston, IL, the most frequently searched job titles are:
What job categories do people searching Study Com jobs in Evanston, IL look for? The top searched job categories for Study Com jobs in Evanston, IL are:
What cities near Evanston, IL are hiring for Study Com jobs? Cities near Evanston, IL with the most Study Com job openings:
Study Com jobs near you
Infographic showing various Study Com job openings in Evanston, IL as of July 2026, with employment types broken down into 1% As Needed, 77% Full Time, 17% Part Time, 1% Temporary, and 4% Contract. Highlights an 95% Physical, 2% Hybrid, and 3% Remote job distribution, with an average salary of $120,236 per year, or $57.8 per hour.

Epidemiology Study Operations Manager

AbbVie

North Chicago, IL • On-site, Remote

$109K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 12 days ago

AbbVie rating

8.7

Company rating: 8.7 out of 10

Based on 100 frontline employees who took The Breakroom Quiz

14th of 86 rated pharmaceutical

Job description

Company Description
About AbbVie
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.
Job Description
Purpose:
This position reports into the Clinical Sciences (CS) Product Office within the Clinical Science organization's Global Strategic Operations. The CS Product Office, Product Safety Team (PST) and Epidemiology organizations work collaboratively and strategically with colleagues across the product lifecycle to identify, evaluate, understand and communicate the safety profile of our drugs to protect patients worldwide.
The PST is a high-profile high-impact team that leads and owns safety decisions and strategy across the product lifecycle. The team partners with stakeholders across the product lifecycle to provide innovative safety-driven strategies, which will maximize product benefit-risk for patients. The CS Product Office plays a critical role in shaping and driving the priorities of the PST by providing strategic and operational leadership oversight of the PST model.
As an Epidemiology Study Operations Manager within the CS Product Office, you will support and partner with the Global Epidemiology organization to achieve its mission in managing the lifecycle of studies utilizing real world evidence and to ensure compliance with quality standards (Global Regulations and AbbVie policies and procedures).
Responsibilities:
  • Strategic management and oversight of Epidemiology-led non interventional studies with progressive autonomy
  • Provide support to the Study Leader for vendor selection, scope development, management, and oversight of external vendors/CROs
  • Manage and coordinate the development of study-related deliverables including development of project plans/timelines, confirming accountabilities, document quality, driving completion of actions and escalating obstacles/risks
  • Drive study-related deliverables to ensure regulatory and process timelines are met
  • Responsible for relevant updates to the cross-functional team and stakeholders on study status
  • Leverage applicable systems and processes to enable successful tracking and completion of the study and study-related deliverables
  • Coordinate the development, review and approval of study protocol and other study-related documents
  • Maintain study-related documents (e.g., meeting minutes, IRB/EC approvals) in the appropriate document repository
  • Responsible for oversight of funds spent against approved budget
  • Proactively identify, address and escalate, as appropriate, project-related issues
  • Identify opportunity areas for efficiency and participate in department related projects in order to achieve operational excellence within Global Epidemiology and the CS Product Office
  • Build solid foundation in understanding regulations and applies knowledge or regulations to guide the development study-related deliverables
  • Collaborate effectively to build and leverage relationships across functions and organizations to achieve business results
  • Participate in audit and inspection preparation and execution activities

Qualifications
  • Bachelor's degree in biological/medical science or healthcare professional
  • 6+ years of experience working in healthcare, research institution, or pharmaceutical industry
  • A minimum of 2 years driving project management activities or operational experience within global companies
  • Preferred experience in one of the following areas: drug development, non-interventional study lifecycle management, risk management, and/or Pharmacovigilance
  • Demonstrated ability to work and collaborate with others to build/leverage relationships
  • Ability to adopt process and technology changes
  • Familiarity with medical and study terminology and concepts is desirable
  • Proficiency in computer skills (Windows, Word, Excel) and in databases (e.g., clinical trial management system)

Additional Information
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
  • The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
  • We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
  • This job is eligible to participate in our long-term incentive programs.

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company's sole and absolute discretion, consistent with applicable law.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
https://www.abbvie.com/join-us/reasonable-accommodations.html

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About AbbVie

Sourced by ZipRecruiter

AbbVie's mission is to discover and deliver innovative medicines that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas: immunology, oncology, neuroscience, eye care, virology, women's health, and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube, and LinkedIn.

Industry

Scientific research and development services

Company size

10,000+ Employees

Headquarters location

North Chicago, IL, US

Year founded

2013

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