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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 ...

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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 12, 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% Internship, 1% As Needed, 87% Full Time, 9% Part Time, and 2% Contract. Highlights an 87% Physical, 4% Hybrid, and 9% Remote job distribution, with an average salary of $80,570 per year, or $38.7 per hour.

Clinical Research Coordinator

Cardiovascular Associates of America

The Villages, FL • On-site

$20.75 - $27.75/hr

Full-time

Posted yesterday

New

Job description

Clinical Research Coordinator
Location: The Villages, Florida
Job Type: Full-time
This is an onsite position in The Villages, FL
About CVAUSA
Cardiovascular Associates of America (CVAUSA) is a rapidly growing leader in cardiovascular care, committed to advancing medical research and improving patient outcomes. As part of our expansion, we are increasing our clinical trial operations and are seeking dynamic, results-driven professionals to join our team in The Villages, Fl.
At CVAUSA, we are focused on innovation and excellence in cardiovascular research, and we believe the best results come from individuals who are passionate about making a difference.
We are hiring a Clinical Research Coordinator for The Village, Fl office. The Clinical Research Coordinator will be responsible for supporting the growth and development of the research program while collaborating with clinic staff on existing and new clinical trials. As part of CVAUSA's national network, this role offers the opportunity to collaborate with teams across the country and make an impact both locally and nationwide.
Position Overview
As a Clinical Research Coordinator, you will play a key role in coordinating and overseeing clinical trials and supporting site operations. You will have the opportunity to manage your studies with a high degree of autonomy while working closely with investigators, sponsors, and site staff. This is an excellent opportunity for a motivated, detail-oriented individual who thrives in a fast-paced environment.
Key Responsibilities
Clinical Trial Coordination
Coordinate all aspects of clinical trials, including patient recruitment, screening, enrollment, and follow-up visits. Ensure study protocols are followed accurately and consistently.
Site Operations
Support day-to-day research site operations while ensuring compliance with regulatory requirements and study protocols.
Data Management
Collect, verify, and maintain clinical trial data, ensuring accuracy, completeness, and timely entry.
Communication & Reporting
Serve as a primary point of contact for study sponsors, participants, and research stakeholders. Provide regular study updates and assist with reporting requirements.
Regulatory Compliance
Maintain up-to-date study documentation, regulatory binders, and patient records in compliance with GCP, ICH guidelines, and applicable regulations.
Process Improvement
Assist with identifying opportunities to improve research workflows and enhance study performance.
What We're Looking For
Detail-Oriented & Organized
Able to manage multiple priorities while maintaining a high level of accuracy and quality.
Strong Communicator
Effectively communicates with sponsors, investigators, site staff, and participants.
Collaborative Team Player
Works well independently and as part of a multidisciplinary team.
Adaptable & Results-Oriented
Thrives in a dynamic environment and remains focused on achieving study goals.
Experience & Qualifications
  • Clinical experience in cardiovascular medicine in a licensed role (e.g., RN, technologist, medical assistant, etc.)
  • Bachelor's degree in a relevant field (life sciences, healthcare, or clinical research) preferred
  • Minimum of 1-2 years of clinical research experience, including patient enrollment and study coordination
  • Strong organizational and time management skills
  • Clinical research certification (e.g., CCRP) preferred
  • Knowledge of GCP, ICH guidelines, and regulatory requirements
  • Experience with electronic data capture systems and regulatory documentation preferred
Why CVAUSA?
At CVAUSA, we believe in the power of innovation and are looking for professionals eager to make an impact in cardiovascular research. As part of our growing organization, you'll be at the forefront of cutting-edge clinical trials.

Apply