Lead Research Coordinator
Lead Clinical Research Coordinator
Location: Orlando, 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 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 Overview
As 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 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 activities comply 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 point of contact for study sponsors, participants, and stakeholders. Provide regular updates and progress 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.
What We’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 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