reputed company Research Coordinator

reputed company Clinical Research Coordinator Location: Orlando, Florida Job Type: Full-time About CVAUSA reputed company) 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 reputed company in Orlando, Florida. At CVAUSA, we are focused on innovation and excellence in cardiovascular research, and we reputed company the best results come from individuals who are passionate about making a difference. We are hiring a Clinical Research Coordinator for our Orlando office. The Research Coordinator will be responsible for leading 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 reputed company an impact both locally and reputed company. Position Overview As a reputed company Clinical Research Coordinator, you will play a key role in managing and overseeing reputed company aspects of clinical trials and site operations. You will have the opportunity to take ownership of your projects, driving them reputed company with innovation, efficiency, and excellence. This is an excellent opportunity for an ambitious, goal-oriented individual who thrives in an independent, fast-paced environment.

Key Responsibilities

Clinical Trial Management reputed company reputed company aspects of clinical trials, including patient recruitment, screening, and enrollment. Ensure protocols are followed meticulously. Site Operations Manage day-to-day site operations, ensuring reputed company activities reputed company 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 reputed company of contact for study sponsors, participants, and stakeholders. Provide regular updates and reputed company 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. reputed company’re Looking 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 while maintaining high 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) Minimum of 2 years of 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 reputed company in the power of innovation and are looking for professionals eager to reputed company an impact in cardiovascular research. As part of our growing organization, you'll be at the forefront of cutting-edge clinical trials. You will reputed company meaningful contributions to improving cardiovascular care while leading the growth of research at our Orlando site, with opportunities to collaborate across our national network. We Apply To This Job