Research Coordinator

Cardiovascular Associates of America; Tucker (GA); On-site; USD 55,000 - 75,000; Full time

Benefits offered by this job

Competitive compensation

Flexible working hours

Supportive, dynamic environment

Job summary

Cardiovascular Associates of America in Tucker, GA, is seeking a Clinical Research Coordinator to oversee clinical trials and support site operations. This onsite position requires coordination of patient recruitment and adherence to study protocols.

The ideal candidate will have clinical experience, a relevant bachelor's degree, and strong organizational and communication skills. CVAUSA offers competitive compensation and opportunities to collaborate nationally.

Qualifications

• Minimum of 1-2 years of clinical research experience, including patient enrollment and study coordination.
• Knowledge of GCP, ICH guidelines, and regulatory requirements.
• Clinical research certification (e.g., CCRP) preferred.

Responsibilities

• Coordinate all aspects of clinical trials, including patient recruitment, screening, and follow-up visits.
• Support day-to-day research site operations ensuring compliance with regulatory requirements.
• Collect, verify, and maintain clinical trial data for accuracy and completeness.
• Serve as a primary point of contact for study sponsors and participants.
• Maintain up-to-date study documentation and patient records in compliance with regulations.

Skills

Clinical experience in cardiovascular medicine

Organizational skills

Time management skills

Strong communication skills

Collaboration skills

Adaptability

Education

Bachelor's degree in life sciences, healthcare or clinical research

Tools

Electronic data capture systems

Job description

Location: Tucker, GA

Job Type: Full-time

Site Information

This is an onsite position in Tucker, GA. 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 Canton, 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 our 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 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.

You will make meaningful contributions to improving cardiovascular care while supporting research initiatives at our Canton, GA 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.