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Contract Cardiovascular Research Jobs (NOW HIRING)

Vitalief

Clinical Research Coordinator

Newark, NJ · On-site

$65 - $78/hr

... cardiovascular research, and the ability to work independently while serving as the primary ... Contracts & Budget Support * Assist with clinical trial agreement (CTA) coordination and ...

Vitalief

Clinical Research Coordinator

Newark, NJ · On-site

$65K - $78K/yr

... cardiovascular research, and the ability to work independently while serving as the primary ... Contracts & Budget Support * Assist with clinical trial agreement (CTA) coordination and budget ...

Vitalief

Clinical Research Coordinator

Newark, NJ · On-site

$65K - $78K/yr

... cardiovascular research, and the ability to work independently while serving as the primary ... Contracts & Budget Support * Assist with clinical trial agreement (CTA) coordination and budget ...

JES Tech

Research Nurse

Houston, TX · On-site

On the Human Health and Performance Contract 2 we are at the forefront of safeguarding astronaut ... We are seeking a Research Nurse for the Cardiovascular & Vision Laboratory at the NASA Johnson ...

JES Tech

Research Nurse

Houston, TX · On-site

On the Human Health and Performance Contract 2 we are at the forefront of safeguarding astronaut ... We are seeking a Research Nurse for the Cardiovascular & Vision Laboratory at the NASA Johnson ...

Cardiovascular Research Foundation

$75 - $85/hr

Support live case sessions, coordinating contracts, HIPAA forms, vendor communications, and grant invoices. * Call for Science (CFS) Responsibilities * Serve as a point of contact for CFS presenters ...

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How much do contract cardiovascular research jobs pay per hour?

As of Sep 4, 2026, the average hourly pay for contract cardiovascular research in the United States is $32.74, according to ZipRecruiter salary data. Most workers in this role earn between $21.63 and $39.90 per hour, depending on experience, location, and employer.

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Contract Cardiovascular Research jobs near you

Clinical Research Coordinator I/II

Medasource

Milwaukee, WI • On-site

$35 - $42/hr

Contractor

Posted 12 days ago

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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