Lead Research Coordinator

Cardiovascular Associates of America - CVAUSA; Orlando (FL); On-site; USD 60,000 - 80,000; Full time

Job summary

Cardiovascular Associates of America (CVAUSA) is seeking a Lead Clinical Research Coordinator in Orlando, Florida. The role requires managing and overseeing clinical trials and site operations with a focus on regulatory compliance and patient recruitment.

The ideal candidate will have a bachelor's degree in a relevant field, clinical experience in cardiovascular medicine, and strong leadership skills. Join us to improve cardiovascular care and contribute to groundbreaking research.

Qualifications

• Clinical experience in cardiovascular medicine in a licensed role.
• Minimum of 2 years of experience managing clinical trials.
• Clinical research certification (e.g., CCRP) preferred.

Responsibilities

• Oversee all aspects of clinical trials, including patient recruitment.
• Manage day-to-day site operations ensuring compliance.
• Collect and manage clinical trial data for accuracy.

Skills

Strong leadership

Effective communication

Problem-solving

Detail-oriented

Education

Bachelor’s degree in a relevant field

Tools

Knowledge of GCP and ICH guidelines

Job description

Cardiovascular Associates of America (CVAUSA) is a rapidly growing leader in cardiovascular care, committed to advancing medical research and improving patient outcomes. We are expanding our clinical trial operations in Orlando, Florida, and are seeking a Lead Clinical Research Coordinator to drive growth and oversee all aspects of clinical trials.

Location: Orlando, Florida
Job Type: Full-time

Position Overview

The Lead Clinical Research Coordinator will manage and oversee clinical trials and site operations, ensuring regulatory compliance, efficient data management, and successful recruitment. The role requires strong leadership, communication, and problem‑solving skills in a fast‑paced environment.

Key Responsibilities

• Oversee all aspects of clinical trials, including patient recruitment, screening, and enrollment.
• Manage day‑to‑day site operations and ensure compliance with regulatory requirements and study protocols.
• Collect, verify, and manage clinical trial data for accuracy and completeness.
• Serve as primary point of contact for study sponsors, participants, and stakeholders; provide regular updates and progress reports.
• Maintain documentation for regulatory submissions and patient records in compliance with ethical and legal standards.
• Identify opportunities for process improvement and implement solutions to enhance efficiency and trial performance.

What We’re Looking For

• Goal‑driven and independent, thrives in an autonomous environment.
• Innovative and results‑oriented, eager to contribute to growth.
• Detail‑oriented and organized, able to manage multiple priorities while maintaining high quality.
• Strong communicator, effectively communicating 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, you’ll 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.