Clinical Research Associate - Study Coordination

UF Health; Jacksonville (FL); On-site; USD 40,000 - 80,000; Full time

Job summary

An established industry player is seeking a Clinical Research Coordinator to assist in the conduct of clinical trials. This role involves ensuring compliance with clinical protocols, coordinating patient visits, and maintaining regulatory documents. Ideal candidates will have strong organizational skills, proficiency in Microsoft Office, and a passion for research. Join a dynamic team dedicated to advancing healthcare through innovative research practices. If you thrive in a fast-paced environment and are eager to contribute to meaningful projects, this opportunity is perfect for you.

Qualifications

• 1 year of professional experience required; 2 years in research regulatory preferred.
• Demonstrated self-motivation and ability to work independently.

Responsibilities

• Assist in clinical trials, ensuring compliance with protocols and guidelines.
• Coordinate patient scheduling and maintain accurate clinical trial documents.

Skills

Microsoft Office proficiency

Critical thinking

Organizational skills

Literature searches

Statistical analysis

Self-motivation

Ability to work under pressure

Education

Bachelor's in Health Sciences

Bachelor's in Public Health

Bachelor's in Research and Statistics

Tools

Adobe Acrobat

Database management software

Job description

An established industry player is seeking a Clinical Research Coordinator to assist in the conduct of clinical trials. This role involves ensuring compliance with clinical protocols, coordinating patient visits, and maintaining regulatory documents. Ideal candidates will have strong organizational skills, proficiency in Microsoft Office, and a passion for research. Join a dynamic team dedicated to advancing healthcare through innovative research practices. If you thrive in a fast-paced environment and are eager to contribute to meaningful projects, this opportunity is perfect for you.