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Research Study Coordinator Jobs in Racine, WI (NOW HIRING)

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Research Study Coordinator information

See Racine, WI salary details

$20.2K

$75.5K

$105.5K

How much do research study coordinator jobs pay per year?

As of Jul 26, 2026, the average yearly pay for research study coordinator in Racine, WI is $75,549.00, according to ZipRecruiter salary data. Most workers in this role earn between $57,200.00 and $93,300.00 per year, depending on experience, location, and employer.

What is the difference between Research Study Coordinator vs Research Assistant?

AspectResearch Study CoordinatorResearch Assistant
CredentialsBachelor's degree often required; certification optionalTypically requires a bachelor's degree or current student status
Work EnvironmentLeads study activities, manages protocols, interacts with staff and participantsSupports data collection, performs administrative tasks, assists with experiments
Employer & Industry UsageUsed in clinical research, academic, and healthcare settingsCommon in research labs, universities, and clinical trials

The Research Study Coordinator and Research Assistant roles often overlap in credentials and work environments, but coordinators typically have more responsibility in managing study protocols and participant interactions. Both roles are essential in research settings, with coordinators taking a leadership role in study execution.

What are Research Study Coordinators?

Research Study Coordinators are professionals responsible for managing and overseeing the day-to-day operations of clinical trials or research studies. They ensure that studies are conducted according to protocols, regulatory guidelines, and ethical standards. Their duties often include recruiting and enrolling participants, collecting and managing data, coordinating with research teams, and maintaining accurate documentation. Research Study Coordinators play a crucial role in ensuring the integrity and success of research projects.

What are some typical challenges faced by Research Study Coordinators when managing multiple clinical trials simultaneously?

Research Study Coordinators often juggle several studies at once, which requires exceptional organizational and time-management skills. Common challenges include keeping meticulous records for each trial, ensuring protocol compliance, and coordinating schedules among investigators, sponsors, and participants. Managing regulatory documentation and staying updated with changing study protocols can also be demanding. Successful coordinators proactively communicate with their teams and utilize digital tools to streamline processes, ensuring each study stays on track.

What are the key skills and qualifications needed to thrive as a Research Study Coordinator, and why are they important?

To thrive as a Research Study Coordinator, you need a background in life sciences or health-related fields, experience with research protocols, and often a bachelor's or master's degree. Familiarity with data management systems, regulatory compliance platforms (such as IRB software), and sometimes certifications like CCRC are typically required. Strong organizational abilities, attention to detail, and effective communication help manage study logistics and participant interactions. These skills are important to ensure studies run efficiently, data is accurate, and compliance with ethical and regulatory standards is maintained.
What job categories do people searching Research Study Coordinator jobs in Racine, WI look for? The top searched job categories for Research Study Coordinator jobs in Racine, WI are:
What cities near Racine, WI are hiring for Research Study Coordinator jobs? Cities near Racine, WI with the most Research Study Coordinator job openings:
Research Study Coordinator jobs near you
Infographic showing various Research Study Coordinator job openings in Racine, WI as of July 2026, with employment types broken down into 1% As Needed, 79% Full Time, 16% Part Time, 1% Temporary, and 3% Contract. Highlights an 96% Physical, 2% Hybrid, and 2% Remote job distribution, with an average salary of $75,549 per year, or $36.3 per hour.
Clinical Study Coordinator

Clinical Study Coordinator

Cancer Treatment Centers of America

Zion, IL • On-site

Full-time

This job post has expired today. Applications are no longer accepted.

Job description

Clinical Study Coordinator
About City of Hope,
City of Hope's mission is to make hope a reality for all touched by cancer and diabetes. Founded in 1913, City of Hope has grown into one of the largest and most advanced cancer research and treatment organizations in the U.S., and one of the leading research centers for diabetes and other life-threatening illnesses. City of Hope research has been the basis for numerous breakthrough cancer medicines, as well as human synthetic insulin and monoclonal antibodies. With an independent, National Cancer Institute-designated comprehensive cancer center that is ranked top 5 in the nation for cancer care by U.S. News & World Report at its core, City of Hope's uniquely integrated model spans cancer care, research and development, academics and training, and a broad philanthropy program that powers its work. City of Hope's growing national system includes its Los Angeles campus, a network of clinical care locations across Southern California, a new cancer center in Orange County, California, and cancer treatment centers and outpatient facilities in the Atlanta, Chicago and Phoenix areas.
The successful candidate:
Hours: Monday - Friday, 7:30 AM - 4:00 PM
Primary Reporting Location: Onsite at Zion, IL (Not a remote position)
Travel Requirement: Must be able to travel to North Shore and Downtown locations as needed. Travel to other locations is less than 20% of the role.
Job Summary:
Under the supervision of the director of Clinical Research and/or Research Manager, the Clinical Study Coordinator plays a key role in supporting oncology clinical trials, ranging from First-in-Human to Phase III studies, as well as Therapeutic Investigator-Initiated Trials (IITs). This position ensures strict adherence to federal regulations, institutional policies, and standard operating procedures (SOPs), while maintaining accurate and timely data collection and documentation.
Key Responsibilities:
  • Coordinate therapeutic clinical trials across various oncology disease areas.
  • Ensure compliance with study protocols, regulatory requirements, and institutional guidelines.
  • Collaborate with investigators on subject recruitment, pre-screening, and enrollment.
  • Present study information to participants, obtain informed consent, and coordinate clinical care.
  • Monitor and document subject condition changes and adverse events.
  • Maintain regulatory documentation and participate in off-site meetings as needed.
  • Provide education and training to clinical staff on research protocols and procedures.
  • Develop study-specific tools and manage biological specimen collection, processing, and shipping.
  • Maintain inventory and ensure equipment certifications are current.

Qualifications:
Education:
  • Bachelor's degree in science, Health, or a related field.
  • In lieu of a degree, 3 additional years of relevant experience may be considered.

Experience:
  • Minimum of 2 years in clinical research or related clinical experience.
  • Preferred: 3+ years in oncology research or experience with Phase I trials.

Certifications:
  • Required within 1 month of hire: IATA, GCP, HSP, and BLS.
  • Required within 1 year of hire: ACRP or SOCRA certification.

Skills and Abilities:
  • Strong technical and critical thinking skills.
  • Excellent problem-solving and decision-making capabilities.
  • Ability to work independently and exercise sound judgment.
  • Effective communication and interpersonal skills.
  • Ability to mentor and train clinical support staff.

City of Hope is an equal opportunity employer.
City of Hope employees pay is based on the following criteria: work experience, qualifications, and work location.

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