Research Coordinator

Cardiovascular Associates of America•Brandon, FL

1d•Onsite

About The Position

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 quickly increasing our clinical trial operations and looking for dynamic, results-driven professionals to join our team at the location in Brando, Florida . At CVAUSA, we are focused on innovation and excellence in cardiovascular research, and we believe that the best results come from individuals who are passionate about making a difference. We are hiring a Clinical Research Coordinator for the Brandon Office. The Research Coordinator will be responsible to lead the growth and development of the research program while also working with other clinic staff on existing and new clinical trials. As part of CVAUSA’s national network, the Clinical Research Coordinator will have the opportunity to collaborate with teams across the country, making an impact on cardiovascular care both locally and nationwide. 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 a fantastic opportunity for an ambitious, goal-oriented individual who thrives in an independent, fast-paced environment.

Requirements

Clinical experience in cardiovascular medicine in any licensed role (i.e. RN, technologist, medical assistant, etc.)
Bachelor’s degree in a relevant field (e.g., life sciences, healthcare, or clinical research)
Experience managing clinical trials, leading the enrollment for multiple clinical trials, developing a research program
Strong organizational and time management skills
Strong Communicator: You can effectively communicate with stakeholders at all levels, including sponsors, site staff, and participants.

Nice To Haves

Clinical research certification (e.g., CCRP)
Knowledge of GCP, ICH guidelines, and regulatory requirements

Responsibilities

Clinical Trial Management: Oversee all aspects of clinical trials, including patient recruitment, screening, and enrollment. Ensure that protocols are followed meticulously.
Site Operations: Handle day-to-day site management, ensuring that all activities comply with regulatory requirements and study protocols.
Data Management: Collect, verify, and manage clinical trial data, ensuring it is accurate and complete.
Communication & Reporting: Act as the primary point of contact for study sponsors, participants, and other stakeholders. Provide regular updates and progress reports.
Regulatory Compliance: Ensure all documentation, including regulatory submissions and patient records, are kept up-to-date and in compliance with ethical and legal standards.
Problem Solving & Innovation: Identify areas for process improvement and implement solutions to drive efficiency and enhance trial operations.