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Cardiovascular Research Assistant Jobs in Wisconsin

WI ยท On-site

$100 - $150/hr

... cardiovascular, aortic surgery domains. Job Duties * Lead the endโ€‘toโ€‘end buildout of the VITAL Lab, including infrastructure, governance, and research roadmap. * Develop a worldโ€‘class AI ...

Assistant Professor (CHS) Job Summary: The Department of Radiology offers a unique opportunity for ... Opportunities for collaborative research and partnerships with industry. * Protected teaching time ...

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Cardiovascular Research Assistant information

See Wisconsin salary details

$8

$26

$61

How much do cardiovascular research assistant jobs pay per hour?

As of Aug 26, 2026, the average hourly pay for cardiovascular research assistant in Wisconsin is $26.69, according to ZipRecruiter salary data. Most workers in this role earn between $15.36 and $30.29 per hour, depending on experience, location, and employer.

What is a cardiovascular research assistant?

Cardiovascular Research Assistants are professionals who support scientific studies focused on the heart and blood vessels. They assist researchers and medical teams by collecting and analyzing data, conducting experiments, maintaining laboratory equipment, and ensuring compliance with research protocols. Their work is essential for advancing understanding and treatment of cardiovascular diseases. They may also help with patient recruitment, data entry, and preparing research documentation.

What are the key skills and qualifications needed to thrive as a cardiovascular research assistant?

To thrive as a Cardiovascular Research Assistant, you need a solid background in biological sciences, research methodology, and data analysis, typically supported by a bachelor's degree in a related field. Familiarity with laboratory equipment, data management systems, and statistical software like SPSS or R is commonly required. Attention to detail, strong organizational skills, and effective communication set candidates apart in this role. These skills are crucial for ensuring accurate research results, maintaining regulatory compliance, and contributing effectively to multidisciplinary research teams.

What are some common challenges faced by cardiovascular research assistants when coordinating clinical trials?

Cardiovascular Research Assistants often face challenges such as managing large volumes of patient data, ensuring strict adherence to study protocols, and coordinating between various stakeholders like physicians, patients, and regulatory bodies. Balancing administrative duties with hands-on research tasks can be demanding, especially when working on multiple studies simultaneously. Effective communication, attention to detail, and strong organizational skills are essential to navigate these challenges and ensure the success of clinical trials.

What is the difference between Cardiovascular Research Assistant vs Cardiovascular Technician?

AspectCardiovascular Research AssistantCardiovascular Technician
Required CredentialsTypically requires a bachelor's degree in health sciences or related field; some roles may need certificationUsually requires a certification or diploma in cardiovascular technology or related field
Work EnvironmentResearch labs, hospitals, academic institutionsHospitals, clinics, diagnostic labs
Employer & Industry UsageResearch institutions, universities, healthcare research departmentsHospitals, cardiology clinics, diagnostic centers
Common Search & Comparison IntentUnderstanding roles in research vs clinical settingsClinical procedures and patient care roles

The main difference between a Cardiovascular Research Assistant and a Cardiovascular Technician lies in their focus and work environment. Research assistants primarily work in labs and academic settings supporting cardiovascular studies, while technicians perform diagnostic procedures directly with patients in clinical settings. Both roles require specialized knowledge, but their day-to-day tasks and career paths differ accordingly.

What are the most commonly searched types of Cardiovascular Research jobs in Wisconsin?

The most popular types of Cardiovascular Research jobs in Wisconsin are:

What are popular job titles related to Cardiovascular Research Assistant jobs in Wisconsin?

For Cardiovascular Research Assistant jobs in Wisconsin, the most frequently searched job titles are:

What job categories do people searching Cardiovascular Research Assistant jobs in Wisconsin look for?

The top searched job categories for Cardiovascular Research Assistant jobs in Wisconsin are:

Infographic showing various Cardiovascular Research Assistant job openings in Wisconsin as of August 2026, with employment types broken down into 2% As Needed, 77% Full Time, 18% Part Time, 1% Temporary, and 2% Contract. Highlights an 98% Physical, 1% Hybrid, and 1% Remote job distribution, with an average salary of $55,519 per year, or $26.7 per hour.

Clinical Research Coordinator I/II

Milwaukee, WI โ€ข On-site

Medasource
Health Care and Social Assistanceย โ€ขย 201 - 500 employees

$35 - $42/hr

Contractor

Posted 3 days ago

New


Job description

Clinical Research Coordinator I/II - Cardiovascular Research
Milwaukee, WI
Hybrid role (approximately 2-3 days/week onsite, dependent on scheduled study visits)
$35 - $42 per hour
Contract: Approximately 6 months, with potential for extension based on study enrollment
ABOUT THE ROLE
Our client is seeking a Clinical Research Coordinator (CRC) I or II to provide full-time support for a hospital-based cardiovascular research study in Milwaukee, WI. This hybrid position involves both remote and onsite work, with onsite presence required approximately 2-3 days per week at depending on study visit schedules. The CRC will play a key role in coordinating day-to-day study activities, with a strong emphasis on patient recruitment, enrollment, and study visit management. The contract is expected to last approximately 6 months, with the possibility of extension based on study enrollment. No RN or other specific clinical license is required for this role.
WHAT YOU'LL DO
  • Coordinate and execute day-to-day activities of an active clinical research study in cardiovascular research.
  • Identify, screen, and recruit potential study participants in accordance with study protocol and eligibility criteria.
  • Coordinate participant enrollment and study-related activities, including scheduling and supporting participant study visits at the clinical research site.
  • Maintain regular communication with study participants and the broader research team.
  • Ensure all study activities are completed in accordance with the protocol, institutional requirements, and applicable clinical research regulations.
  • Maintain accurate and timely study documentation and participant records.
  • Assist with data collection, data entry, and resolution of study-related documentation as needed.
  • Track recruitment and enrollment progress, providing updates to the study team.
  • Coordinate with investigators, clinical staff, research personnel, and other stakeholders to support successful study execution.
  • Perform remote recruitment and administrative activities when onsite presence is not required.
  • Maintain participant confidentiality and adhere to Good Clinical Practice (GCP) and research compliance requirements.
WHAT YOU BRING
  • Previous experience supporting clinical research studies in a Clinical Research Coordinator, Research Coordinator, or similar capacity.
  • Working knowledge of clinical research processes, including participant recruitment, screening, enrollment, study visits, and research documentation.
  • Ability to independently manage study-related responsibilities and competing priorities.
  • Strong organizational, communication, and documentation skills.
  • Comfortable communicating directly with potential and enrolled study participants.
  • Ability to work approximately 40 hours per week.
  • Ability to work onsite at Aurora St. Luke's Medical Center approximately 2-3 days per week, with onsite frequency varying based on scheduled study visits.
  • Preferred: Cardiovascular/cardiology clinical research experience.
  • Preferred: Previous experience coordinating interventional or hospital-based clinical studies.
  • Preferred: Familiarity with Good Clinical Practice (GCP), IRB requirements, and clinical research regulatory standards.
  • Preferred: Experience working within a large health system, hospital, or academic medical center.
  • No RN license or other specific clinical license required.

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