Clinical Research Coordinator III - Mayerson Center (JR222550)

About the role

The Clinical Research Coordinator III will be responsible for managing clinical research projects, ensuring compliance with regulatory standards, and coordinating with investigators and study teams.

Responsibilities

• Manage and coordinate clinical research studies
• Ensure adherence to regulatory guidelines and sponsor requirements
• Collaborate with investigators and study teams to ensure successful project completion
• Prepare and review documents such as informed consents, case report forms, and other regulatory documents
• Oversee data management and quality assurance processes
• Communicate effectively with stakeholders including patients, families, and regulatory bodies

Requirements

• Bachelor’s degree in a related field (e.g., Biomedical Sciences, Public Health)
• Minimum of 5 years of experience in clinical research coordination
• Experience with regulatory submissions and compliance
• Strong organizational and communication skills
• Proficiency in Microsoft Office Suite

Qualifications

• Current certification as a Certified Clinical Research Professional (CCRP) or equivalent
• Knowledge of Good Clinical Practice (GCP) guidelines
• Ability to work independently and manage multiple projects simultaneously

Skills

• Excellent written and verbal communication skills
• Strong attention to detail and ability to manage complex documentation
• Experience with electronic data capture systems (EDC)
• Ability to work under pressure and meet deadlines

Benefits

• Flexible schedule
• Competitive compensation package
• Professional development opportunities
• Health insurance benefits

Pay

$XX.XX per hour

Schedule

Full-time, Monday through Friday, 8:00 AM - 4:30 PM