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RN or LPN Clinical Research Coordinator

Cardiovascular Associates of America - CVAUSA

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 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 areseekingdynamic, 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. We are hiring a Clinical Research Coordinator for our Palm Beach Gardens office. The Research Coordinator willbe responsible forleading the growth and development of the research program while also 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 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 whothrivesin an independent, fast-paced environment. Key Responsibilities: 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 activitiescomply withregulatory 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:Maintainup-to-date documentation, including regulatory submissions and patient records, in compliance with ethical and legal standards. Problem Solving & Innovation:Identifyopportunities for process improvement and implement solutions to enhance efficiency and trial performance. WhatWe’reLooking For: 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 whilemaintaininghigh quality. Strong Communicator:Effectively communicates with sponsors, site staff, and participants. Experience & Qualifications: 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 Why CVAUSA? At CVAUSA, we believe in the power of innovation and are looking for professionals eager to make an impactincardiovascular research. As part of our growing organization,you’llbe at the forefront ofcutting-edgeclinical 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. #J-18808-Ljbffr Cardiovascular Associates of America - CVAUSA

Vacancy posted 2 days ago
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