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How much do cardiovascular research manager jobs pay per hour?

As of Jun 26, 2026, the average hourly pay for cardiovascular research manager in the United States is $49.74, according to ZipRecruiter salary data. Most workers in this role earn between $38.94 and $58.89 per hour, depending on experience, location, and employer.

What does a Cardiovascular Research Manager do?

A Cardiovascular Research Manager oversees and coordinates research projects related to heart and vascular health. They manage research teams, develop study protocols, ensure compliance with regulatory requirements, and handle budgets and schedules. Their role is crucial in advancing knowledge and treatments in cardiovascular medicine, often collaborating with physicians, scientists, and sponsors. By managing the logistics and administration of clinical trials or laboratory studies, they help ensure research is conducted efficiently, ethically, and safely.

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

To thrive as a Cardiovascular Research Manager, you need a solid background in biomedical sciences, clinical research experience, and often an advanced degree such as a PhD, MD, or MPH. Familiarity with clinical trial management systems, regulatory compliance frameworks (like GCP and FDA guidelines), and data analysis tools is essential. Strong leadership, communication, and organizational skills help manage multidisciplinary teams and complex research projects effectively. These competencies ensure the successful design, execution, and oversight of cardiovascular research that meets ethical, regulatory, and scientific standards.

What are some common challenges faced by a Cardiovascular Research Manager, and how can they be addressed?

Cardiovascular Research Managers often encounter challenges such as coordinating multi-disciplinary teams, ensuring compliance with strict regulatory requirements, and managing complex clinical trial protocols. Balancing administrative duties with scientific oversight can also be demanding. Effective communication, strong organizational skills, and staying updated on the latest regulatory guidelines are essential strategies for addressing these challenges. Building a collaborative team environment and leveraging project management tools can also help streamline operations and improve research outcomes.
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Cardiovascular Research Manager jobs near you
RN or LPN Clinical Research Coordinator

RN or LPN Clinical Research Coordinator

Cardiovascular Associates of America

Palm Beach Gardens, FL • On-site

$65K - $81K/yr

Full-time

Posted 15 days ago

Job description

Job Title: Clinical Research Coordinator 
Location: Palm Beach Gardens, FL 
This is not a remote position. This is an in-person position in Palm Beach Gardens, Florida

Job Type: Full-time 

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 Palm Beach Gardens, Florida. 

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 our Palm Beach Gardens office. The Research Coordinator will be responsible for leading the growth and development of the research program while also 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 managing and overseeing all aspects of clinical trials and site operations. You will have the opportunity to take ownership of your projects, driving them forward with innovation, efficiency, and excellence. This is an excellent opportunity for an ambitious, goal-oriented individual who thrives in an independent, fast-paced environment. 

Key Responsibilities: 

  • Clinical Trial Management: Oversee all aspects of clinical trials, including patient recruitment, screening, and enrollment. Ensure protocols are followed meticulously.  

  • Site Operations: Manage day-to-day site operations, ensuring all activities comply with regulatory requirements and study protocols.  

  • Data Management: Collect, verify, and manage clinical trial data, ensuring accuracy and completeness.  

  • Communication & Reporting: Serve as the primary point of contact for study sponsors, participants, and stakeholders. Provide regular updates and progress reports.  

  • Regulatory Compliance: Maintain up-to-date documentation, including regulatory submissions and patient records, in compliance with ethical and legal standards.  

  • Problem Solving & Innovation: Identify opportunities for process improvement and implement solutions to enhance efficiency and trial performance.  

What We’re Looking For: 

  • Goal-Driven & Independent: Thrives in an autonomous environment and takes ownership of responsibilities.  

  • Innovative & Results-Oriented: Eager to contribute to growth and bring effective solutions.  

  • Detail-Oriented & Organized: Able to manage multiple priorities while maintaining high quality.  

  • Strong Communicator: Effectively communicates with sponsors, site staff, and participants.  

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)  

  • Experience managing clinical trials, leading enrollment, and developing research programs  

  • Strong organizational and time management skills  

  • Clinical research certification (e.g., CCRP) preferred  

  • Knowledge of GCP, ICH guidelines, and regulatory requirements  

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. 

You will make meaningful contributions to improving cardiovascular care while leading the growth of research at our Palm Beach Gardens site, with opportunities to collaborate across our national network. We offer competitive compensation, flexible working hours, and a supportive, dynamic environment where your contributions are valued. 

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