Clinical Research Coordinator

Job Title: Clinical Research Coordinator Location: Orlando, Florida Job Type: Full-time This is an onsite positionin Orlando We arehiring a Clinical Research Coordinator forthe Orlando Office. TheResearch Coordinator will be responsibletoleadthe growth and development of the research programwhile 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. Position Overview As a Clinical ResearchCoordinatoryou 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 whothrivesin an independent, fast-paced environment. Key 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. What We’re Looking For Goal-Driven & Independent: You thrive in an autonomous work environment and take full ownership of your responsibilities. Innovative & Results-Driven: You are eager to contribute to CVAUSA’s rapid growth and bring fresh, effective solutions to the table. Detail-Oriented & Highly Organized: You have the ability to manage multiple tasks and deadlines without sacrificing quality. Strong Communicator: You can effectively communicate with stakeholders at all levels, including sponsors, site staff, and participants. Experience & Qualifications 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 Clinical research certification (e.g., CCRP) is a plus Knowledge of GCP, ICH guidelines, and regulatory requirements #J-18808-Ljbffr