A complete application in a minute
Tailored resume and cover letter, ready to send.
Cardiovascular Associates of America invites applications for a Clinical Research Coordinator to lead clinical trials in Palm Beach Gardens, Florida. The role involves oversight of trial management, patient recruitment, and compliance with regulatory requirements.
Ideal candidates should have clinical experience in cardiovascular medicine, a relevant bachelor's degree, and strong organizational skills. This full-time position offers competitive compensation and professional development opportunities.
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
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.
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.
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.
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.
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
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.