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Entry Level Cardiovascular Research Scientist Jobs

Uw

Managing Research Scientist, CVD

Olympia, WA · On-site

As a Managing Research Scientist, you will independently perform quantitative analyses, contribute ... We are looking for someone to join a new initiative within the Program in Cardiovascular Health ...

New

Children's Mercy KC

Doctoral Research Faculty

Kansas City, MO · On-site

$47K - $64K/yr

... cardiovascular research program that integrates scientific discovery with excellence in pediatric ... patient care. Primary Responsibilities * Serve as Principal Investigator, Co-Investigator, Sub ...

Cardiovascular Associates of America

FL · On-site

Cardiovascular Associates of America (CVAUSA) is a rapidly growing leader in cardiovascular care ... Bachelor's degree in a relevant field (e.g., life sciences, healthcare, or clinical research)

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Entry Level Cardiovascular Research Scientist information

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$50.5K

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$174K

How much do entry level cardiovascular research scientist jobs pay per year?

As of Sep 6, 2026, the average yearly pay for entry level cardiovascular research scientist in the United States is $130,117.00, according to ZipRecruiter salary data. Most workers in this role earn between $107,500.00 and $173,000.00 per year, depending on experience, location, and employer.

What cities are hiring for Entry Level Cardiovascular Research Scientist jobs?

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

The most popular types of Cardiovascular Research Scientist jobs are:

Entry Level Cardiovascular Research Scientist jobs near you

Clinical Research Coordinator

Cardiovascular Associates of America

Tucker, GA • On-site

$22.75 - $30.50/hr

Full-time

Posted 11 days ago

Key responsibilities

  • Coordinate all aspects of clinical trials, including patient recruitment, screening, enrollment, and follow-up visits.

  • Support day-to-day research site operations while ensuring compliance with regulatory requirements and study protocols.

  • Collect, verify, and maintain clinical trial data, ensuring accuracy, completeness, and timely entry.

Job description

Clinical Research Coordinator
Location: Tucker, Ga

Job Type: Full-time

This is an onsite position in Tucker, Georgia
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 Tucker, Ga.

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 Tucker, Ga. 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 ResponsibilitiesClinical 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 ForDetail-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.

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