Lead Research Coordinator

About the role

This is in in-person position located in Orlando, Florida.

Key Responsibilities

• Oversee all aspects of clinical trials, including patient recruitment, screening, and enrollment. Ensure protocols are followed meticulously.
• Manage day-to-day site operations, ensuring all activities comply with regulatory requirements and study protocols.
• Collect, verify, and manage clinical trial data, ensuring accuracy and completeness.
• Serve as the primary point of contact for study sponsors, participants, and stakeholders. Provide regular updates and progress reports.
• Maintain up-to-date documentation, including 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.

Qualifications

• 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.
• 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.