Research Coordinator

Cardiovascular Associates of America • Davenport, IA

3d • Onsite

About The Position

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 their expansion, they are quickly increasing clinical trial operations and looking for dynamic, results-driven professionals. The Research Coordinator will be responsible for leading the growth and development of the research program while also working with other clinic staff on existing and new clinical trials. As part of CVAUSA’s national network, the Clinical Research Coordinator will have the opportunity to collaborate with teams across the country, making an impact on cardiovascular care both locally and nationwide. This role involves managing and overseeing all aspects of clinical trials and site operations, with the opportunity to take ownership of projects, driving them forward with innovation, efficiency, and excellence. This is a fantastic opportunity for an ambitious, goal-oriented individual who thrives in an independent, fast-paced environment.

Requirements

• Clinical experience in cardiovascular medicine in any licensed role (i.e. RN, technologist, medical assistant, etc.)
• Bachelor’s degree in a relevant field (e.g., life sciences, healthcare, or clinical research)
• Experience managing clinical trials, leading the enrollment for multiple clinical trials, developing a research program
• Strong organizational and time management skills
• Knowledge of GCP, ICH guidelines, and regulatory requirements

Nice To Haves

• Clinical research certification (e.g., CCRP)

Responsibilities

• Oversee all aspects of clinical trials, including patient recruitment, screening, and enrollment. Ensure that protocols are followed meticulously.
• Handle day-to-day site management, ensuring that all activities comply with regulatory requirements and study protocols.
• Collect, verify, and manage clinical trial data, ensuring it is accurate and complete.
• Act as the primary point of contact for study sponsors, participants, and other stakeholders. Provide regular updates and progress reports.
• Ensure all documentation, including regulatory submissions and patient records, are kept up-to-date and in compliance with ethical and legal standards.
• Identify areas for process improvement and implement solutions to drive efficiency and enhance trial operations.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Number of Employees: 11-50 employees