Lead Research Coordinator at Cardiovascular Associates of America | Torre

Lead Research Coordinator

You'll lead cardiovascular research growth, making a national impact on patient care and innovation.
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Freelance
Recurrent
Compensation is to be agreed upon.
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Remote (for United States residents)
Shared by
Emma of Torre.ai
about 5 hours ago

Requirements and responsibilities


About CVAUSACardiovascular 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 are seeking dynamic, results-driven professionals to join our team in Orlando, 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 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 make an impact both locally and nationwide.Position OverviewAs a Lead 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 who thrives in an independent, fast-paced environment.Key ResponsibilitiesClinical Trial ManagementOversee all aspects of clinical trials, including patient recruitment, screening, and enrollment. Ensure protocols are followed meticulously.Site OperationsManage day-to-day site operations, ensuring all activities comply with regulatory requirements and study protocols.Data ManagementCollect, verify, and manage clinical trial data, ensuring accuracy and completeness.Communication & ReportingServe as the primary point of contact for study sponsors, participants, and stakeholders. Provide regular updates and progress reports.Regulatory ComplianceMaintain up-to-date documentation, including regulatory submissions and patient records, in compliance with ethical and legal standards.Problem Solving & InnovationIdentify opportunities for process improvement and implement solutions to enhance efficiency and trial performance.What We’re Looking ForGoal-Driven & IndependentThrives in an autonomous environment and takes ownership of responsibilities.Innovative & Results-OrientedEager to contribute to growth and bring effective solutions.Detail-Oriented & OrganizedAble to manage multiple priorities while maintaining high quality.Strong CommunicatorEffectively communicates with sponsors, site staff, and participants.Experience & QualificationsClinical 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 programsStrong organizational and time management skillsClinical research certification (e.g., CCRP) preferredKnowledge of GCP, ICH guidelines, and regulatory requirementsWhy CVAUSA?At CVAUSA, we believe in the power of innovation and are looking for professionals eager to make an impact in cardiovascular research. As part of our growing organization, you'll be at the forefront of cutting-edge clinical trials.You will make 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
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