Research Coordinator

Cardiovascular Associates of America•Canton, GA

2d•Onsite

About The Position

Clinical Research Coordinator Location: Canton, GA 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 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 Canton, 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.

Requirements

Clinical experience in cardiovascular medicine in a licensed role (e.g., RN, technologist, medical assistant, etc.)
Minimum of 1–2 years of clinical research experience, including patient enrollment and study coordination
Strong organizational and time management skills
Knowledge of GCP, ICH guidelines, and regulatory requirements

Nice To Haves

Bachelor’s degree in a relevant field (life sciences, healthcare, or clinical research) preferred
Clinical research certification (e.g., CCRP) preferred
Experience with electronic data capture systems and regulatory documentation preferred

Responsibilities

Coordinate all aspects of clinical trials, including patient recruitment, screening, enrollment, and follow-up visits. Ensure study protocols are followed accurately and consistently.
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.
Serve as a primary point of contact for study sponsors, participants, and research stakeholders. Provide regular study updates and assist with reporting requirements.
Maintain up-to-date study documentation, regulatory binders, and patient records in compliance with GCP, ICH guidelines, and applicable regulations.
Assist with identifying opportunities to improve research workflows and enhance study performance.