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Cardiovascular Research Coordinator Jobs (NOW HIRING)

Vitalief

Clinical Research Coordinator

Newark, NJ · On-site

$65K - $78K/yr

... cardiovascular research, and the ability to work independently while serving as the primary ... RESPONSIBILITIES Study Coordination & Participant Management * Manage day-to-day study activities ...

Vitalief

Clinical Research Coordinator

Newark, NJ · On-site

$65K - $78K/yr

... cardiovascular research, and the ability to work independently while serving as the primary ... RESPONSIBILITIES Study Coordination & Participant Management * Manage day-to-day study activities ...

System One

Research Coordinator

Boston, MA · On-site

$25 - $28/hr

Research Coordinator Location: Boston MA Type: Contract To Hire Compensation: $25-$28/hr Contractor ... Conduct medical record screening of cardiovascular in-patients and out-patients to identify ...

System One

Research Coordinator

Boston, MA · On-site

$25 - $28/hr

Research Coordinator Location: Boston MA Type: Contract To Hire Compensation: $25-$28/hr Contractor ... Conduct medical record screening of cardiovascular in-patients and out-patients to identify ...

System One

Research Coordinator

Boston, MA · On-site

$25 - $28/hr

Research Coordinator Location: Boston MA Type: Contract To Hire Compensation: $25-$28/hr Contractor ... Conduct medical record screening of cardiovascular in-patients and out-patients to identify ...

System One

Research Coordinator

Boston, MA · On-site

$25 - $28/hr

Research Coordinator Location: Boston MA Type: Contract To Hire Compensation: $25-$28/hr Contractor ... Conduct medical record screening of cardiovascular in-patients and out-patients to identify ...

System One

Research Coordinator

Boston, MA · On-site

$25 - $28/hr

Research Coordinator Location: Boston MA Type: Contract To Hire Compensation: $25-$28/hr Contractor ... Conduct medical record screening of cardiovascular in-patients and out-patients to identify ...

System One

Research Coordinator

Boston, MA · On-site

$25 - $28/hr

Research Coordinator Location: Boston MA Type: Contract To Hire Compensation: $25-$28/hr Contractor ... Conduct medical record screening of cardiovascular in-patients and out-patients to identify ...

System One

Research Coordinator

Boston, MA · On-site

$25 - $28/hr

Research Coordinator Location: Boston MA Type: Contract To Hire Compensation: $25-$28/hr Contractor ... Conduct medical record screening of cardiovascular in-patients and out-patients to identify ...

System One

Research Coordinator

Boston, MA · On-site

$25 - $28/hr

Research Coordinator Location: Boston MA Type: Contract To Hire Compensation: $25-$28/hr Contractor ... Conduct medical record screening of cardiovascular in-patients and out-patients to identify ...

System One

Research Coordinator

Boston, MA · On-site

$25 - $28/hr

Research Coordinator Location: Boston MA Type: Contract To Hire Compensation: $25-$28/hr Contractor ... Conduct medical record screening of cardiovascular in-patients and out-patients to identify ...

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Cardiovascular Research Coordinator information

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$21.5K

$80.6K

$112.5K

How much do cardiovascular research coordinator jobs pay per year?

As of Aug 9, 2026, the average yearly pay for cardiovascular research coordinator in the United States is $80,570.00, according to ZipRecruiter salary data. Most workers in this role earn between $61,000.00 and $99,500.00 per year, depending on experience, location, and employer.

What is a cardiovascular research coordinator?

Cardiovascular Research Coordinators are professionals who manage and oversee clinical research studies related to heart and vascular health. They handle tasks such as recruiting participants, ensuring compliance with study protocols, collecting and managing data, and coordinating communication between researchers, patients, and regulatory bodies. Their work is essential for advancing medical knowledge and developing new treatments for cardiovascular diseases. They often work in hospitals, universities, or research institutions and must be knowledgeable about clinical trial regulations and patient care.

What are some common challenges faced by a cardiovascular research coordinator during clinical trials?

A Cardiovascular Research Coordinator often manages multiple studies simultaneously, which can present challenges in balancing regulatory compliance, patient recruitment, and data accuracy. Coordinators must ensure all study protocols are strictly followed, which requires close attention to detail and frequent communication with principal investigators, sponsors, and participants. Additionally, recruiting and retaining eligible patients for cardiovascular studies can be demanding due to strict inclusion criteria and complex procedures. Staying updated on regulatory changes and maintaining thorough documentation are also essential parts of the role.

What are the key skills and qualifications needed to thrive as a cardiovascular research coordinator, and why are they important?

To thrive as a Cardiovascular Research Coordinator, you need a background in life sciences or nursing, clinical research experience, and knowledge of cardiovascular medicine. Familiarity with electronic data capture systems, clinical trial management software, and regulatory compliance (such as Good Clinical Practice certification) is typically required. Strong organizational skills, attention to detail, and effective communication are essential soft skills for managing studies and collaborating with multidisciplinary teams. These competencies ensure accurate data collection, regulatory adherence, and successful coordination of complex research protocols.

What is the difference between Cardiovascular Research Coordinator vs Cardiovascular Clinical Research Associate?

AspectCardiovascular Research CoordinatorCardiovascular Clinical Research Associate
CredentialsTypically requires a bachelor's degree in health sciences or related field; certifications like CCRP are commonOften requires a bachelor's degree; certifications such as CCRP or RAC may be preferred
Work EnvironmentWorks in hospitals, research centers, or academic institutions conducting clinical trialsWorks in clinical trial sites, monitoring studies, ensuring protocol compliance
Employer & Industry UsageUsed by hospitals, research institutions, and pharmaceutical companies in cardiovascular studiesEmployed by CROs, pharmaceutical companies, and research sites for trial oversight

While both roles involve supporting cardiovascular clinical research, the Cardiovascular Research Coordinator primarily manages study operations and participant coordination, whereas the Cardiovascular Clinical Research Associate focuses on monitoring trial compliance and data integrity. Both roles require similar credentials and work in related environments, but their specific responsibilities differ.

More about Cardiovascular Research Coordinator jobs
What cities are hiring for Cardiovascular Research Coordinator jobs? Cities with the most Cardiovascular Research Coordinator job openings:
What are the most commonly searched types of Cardiovascular Research jobs? The most popular types of Cardiovascular Research jobs are:
What states have the most Cardiovascular Research Coordinator jobs? States with the most job openings for Cardiovascular Research Coordinator jobs include:
What job categories do people searching Cardiovascular Research Coordinator jobs look for? The top searched job categories for Cardiovascular Research Coordinator jobs are:
Cardiovascular Research Coordinator jobs near you
Infographic showing various Cardiovascular Research Coordinator job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 86% Full Time, 11% Part Time, and 2% Contract. Highlights an 87% Physical, 3% Hybrid, and 10% Remote job distribution, with an average salary of $80,570 per year, or $38.7 per hour.

Clinical Research Coordinator - Cardiovascular

Vitalief

Rahway, NJ • On-site

$65K - $80K/yr

Full-time

Medical, Life, Retirement, PTO

Re-posted 17 hours ago

Job description

ABOUT VITALIEF
Vitalief is a trusted partner to Sponsors, CROs, and Sites across the research and clinical trials landscape. By blending deep subject matter expertise with strong business acumen, we deliver Consulting and Functional Service Provider (FSP) solutions that empower organizations to do more with less, streamlining operations, reducing costs, and accelerating breakthroughs that ultimately benefit patients.
POSITION SUMMARY:
We are looking for an experienced Clinical Research Coordinator (CRC) to join Vitalief as a full-time employee with comprehensive benefits. This role will support cardiovascular clinical trials conducted at community hospital sites and outpatient cardiology clinics in Rahway, New Jersey, as part of large pharmaceutical and device-sponsored studies. The ideal candidate will have at least two years of experience as a CRC, along with strong attention to detail, a genuine interest in cardiovascular research, and the ability to work independently in a fast-paced environment.
This role requires a proactive, self-starting individual who can effectively manage patient-facing responsibilities while ensuring strict adherence to protocol requirements, regulatory standards, and specific cardiovascular diagnostic procedures (such as ECGs, Holter monitoring, and echocardiograms). The CRC will work closely with the Principal Investigator (PI), often a cardiologist, and site leadership to support the successful execution of the study, which may include drug therapies, implantable devices, or interventional procedures.
WHY VITALIEF?
  • Impactful Work: Contribute to scientific advancements that directly improve patient lives in the field of cardiovascular medicine.
  • People-First Culture: Thrive in an environment that fosters growth, innovation, and collaboration.
  • Comprehensive Benefits: Enjoy 20 PTO days, 9 paid holidays, company-paid life insurance, short- and long-term disability, a 401(k) retirement plan, and robust healthcare options.
  • Work Location: On-site (normal business hours Monday through Friday) in Rahway, NJ.
  • Salary Range: $65,000 to $80,000 (depending on experience level).

Responsibilities:
  • Coordinate and execute day-to-day clinical trial activities across sites in accordance with the study protocol, GCP, and regulatory requirements.
  • Work closely with the Principal Investigator (PI) to support study oversight, patient eligibility review, safety reporting, and protocol adherence for cardiovascular trials.
  • Identify, screen, and consent eligible patients for participation in cardiovascular studies, including those involving acute cardiac events or chronic heart conditions.
  • Schedule and manage patient visits, ensuring protocol compliance and timely completion of study procedures such as ECGs, vital signs monitoring, and blood draws.
  • Serve as the primary point of contact for study participants, including meeting patients during visits and conducting follow-up communications.
  • Accurately collect, document, and maintain study data in source documents and electronic systems (e.g., EDC, CTMS).
  • Extract relevant clinical data from Electronic Medical Records (EMR), specifically focusing on cardiology reports, cardiac catheterization results, and echocardiogram findings.
  • Ensure proper specimen collection, processing, storage, and shipment in compliance with protocol and laboratory requirements.
  • Collaborate with investigators, site staff, cardiac cath lab personnel, and sponsor representatives to ensure smooth study conduct.
  • Monitor patient safety and report adverse events per protocol and regulatory guidelines, with a strong understanding of cardiovascular-specific safety reporting.
  • Maintain regulatory binders and ensure audit readiness at all times.
  • Support monitoring visits, audits, and inspections as needed.
  • Manage device accountability for trials involving implantable cardiovascular devices or wearables (e.g., Holter monitors).

Qualifications:
  • Bachelor's degree required (healthcare, life sciences, or related field preferred).
  • Minimum of 2 years of experience as a Clinical Research Coordinator.
  • Prior experience working as a CRC in an Academic Medical Center (AMC) or community hospital setting is strongly preferred.
  • Experience in cardiovascular, cardiology, or vascular research studies is highly preferred.
  • Familiarity with cardiovascular medical terminology and procedures (e.g., ECGs, echocardiograms, Holter monitors, cardiac catheterization).
  • Strong understanding of Good Clinical Practice (GCP) and clinical trial processes.
  • Demonstrated ability to work independently and manage multiple priorities across sites.
  • Enthusiastic and motivated team player; Self-starter with the ability to take initiative.
  • Excellent organizational skills and high attention to detail.
  • Strong interpersonal and communication skills, with a patient-centered approach.
  • Ability to problem-solve and adapt in a dynamic clinical environment.
  • Proficiency with electronic data capture (EDC) systems and Microsoft Office.
  • Ability to travel to other hospital locations local to Rahway, NJ.

PHYSICAL DEMANDS: Standing, sitting, walking, visual perception, talking and hearing. Lifting up to 20lbs. Some travel to hospital locations local to Rahway, NJ.
IMPORTANT NOTE: Vitalief partners with clients such as major medical centers and academic institutions that often requires all on-site resources such as prospective Vitalief consultants to be inoculated annually for Influenza and successfully pass a Mantoux Tuberculin Skin Test (TST) for Mycobacterium Tuberculosis.
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