Cardiovascular Research Coordinator - On-Site Davenport

CVAUSA; Davenport (IA); On-site; USD 55,000 - 75,000; Full time

Benefits offered by this job

Competitive compensation

Flexible working hours

Job summary

CVAUSA, Cardiovascular Associates of America, Davenport, Iowa, is seeking a Clinical Research Coordinator to lead the growth and oversight of our cardiovascular research program. You will manage trials, recruit and screen participants, ensure protocol compliance, and partner with clinic staff to advance state-of-the-art care.

This on-site role emphasizes independence and efficiency in a fast-paced environment.

Qualifications

• Clinical experience in cardiovascular medicine or related clinical support role.
• Bachelor’s degree in life sciences, healthcare, or clinical research.
• Experience managing clinical trials, leading enrollment across multiple studies, and supporting research program development.
• Strong organizational and time management skills.
• Clinical research certification (e.g., CCRP) is a plus.

Responsibilities

• Oversee all aspects of clinical trials, including patient recruitment, screening, and enrollment.
• Handle day-to-day site management, ensuring compliance with regulatory requirements and study protocols.
• Collect, verify, and manage clinical trial data to ensure accuracy and completeness.
• Act as primary contact for study sponsors, participants, and stakeholders with regular updates.
• Ensure all documentation, including regulatory submissions and patient records, is up-to-date and compliant with ethical and legal standards.
• Identify areas for process improvement and implement solutions to drive efficiency and enhance trial operations.

Skills

Clinical trial management

Regulatory compliance

Data management

Communication

Organization

GCP knowledge

Education

Bachelor’s degree in life sciences / healthcare / clinical research

Job description

CVAUSA, Cardiovascular Associates of America, Davenport, Iowa, is seeking a Clinical Research Coordinator to lead the growth and oversight of our cardiovascular research program. You will manage trials, recruit and screen participants, ensure protocol compliance, and partner with clinic staff to advance state-of-the-art care.

This on-site role emphasizes independence and efficiency in a fast-paced environment.