Sr. Lead Clinical Research Coordinator

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 seeking dynamic, results-driven professionals to join our team at the MyCardiologist location in South Miami, Florida. At CVAUSA, we focus on innovation and excellence in cardiovascular research, believing that passionate individuals drive the best results.

About the role

As a Lead Clinical Research Coordinator at MyCardiologist, you will lead 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, you will have the opportunity to collaborate with teams across the country, making an impact on cardiovascular care both locally and nationwide.

You will play a key role in managing and overseeing all aspects of clinical trials and site operations, taking ownership of projects with innovation, efficiency, and excellence. This is a fantastic opportunity for an ambitious, goal-oriented individual who thrives in an independent, fast-paced environment.

Must live in the Lake Nona area or be willing to relocate.

Responsibilities

• Oversee all aspects of clinical trials, including patient recruitment, screening, and enrollment
• Ensure protocols are followed meticulously
• Handle day-to-day site management, ensuring compliance with regulatory requirements and study protocols
• Collect, verify, and manage clinical trial data, ensuring accuracy and completeness
• Act as the primary point of contact for study sponsors, participants, and other stakeholders
• Provide regular updates and progress reports
• Ensure all documentation, including regulatory submissions and patient records, are kept up-to-date and in compliance with ethical and legal standards
• Identify areas for process improvement and implement solutions to drive efficiency and enhance trial operations

Requirements

• Clinical experience in cardiovascular medicine in any licensed role (e.g., RN, technologist, medical assistant)
• Bachelor’s degree in a relevant field (e.g., life sciences, healthcare, or clinical research)
• Experience managing clinical trials, leading enrollment for multiple trials, and developing a research program
• Strong organizational and time management skills
• Clinical research certification (e.g., CCRP) is a plus
• Knowledge of GCP, ICH guidelines, and regulatory requirements

Skills

• Goal-driven and independent, thriving in an autonomous work environment
• Innovative and results-driven, eager to contribute to rapid growth
• Detail-oriented and highly organized, managing multiple tasks and deadlines without sacrificing quality
• Strong communicator, effectively engaging with stakeholders at all levels

Benefits

• Competitive compensation
• Flexible working hours
• Supportive, dynamic environment where contributions are valued
• Opportunities to collaborate with teams nationwide