Clinical Research Coordinator

Company Description

Daytona Beach Vascular Access is dedicated to providing high-quality care and services to patients requiring vascular access solutions. Located in Daytona Beach, FL, our practice prides itself on its commitment to advanced medical procedures and a patient-centered approach. We aim to support both patients and healthcare professionals through excellence in care and operational efficiency. Our team fosters a collaborative environment focused on clinical innovation and improving patient outcomes.

Role Description

This is a part-time, on-site role for a Clinical Research Coordinator based in Daytona Beach, FL. The Clinical Research Coordinator will manage clinical research studies, ensuring protocols and regulatory requirements are adhered to. Key responsibilities include obtaining informed consent from study participants, coordinating clinical trials, monitoring research progress, maintaining accurate documentation, and communicating effectively with the clinical team and study sponsors. The role will involve collaborating with healthcare professionals to ensure the accurate execution of protocols and ethical standards.

Qualifications

·      Strong understanding of Good Clinical Practice (GCP) and regulatory requirements 

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• Experience with Informed Consent processes and ensuring compliance with ethical standards
• Knowledge of Protocol development and adherence
• Proven background in Research and Clinical Research Experience
• Familiarity with the design, implementation, and management of Clinical Trials
• Strong organizational skills with attention to detail
• Effective communication skills, both written and verbal
• Ability to work collaboratively in an on-site clinical environment
• Bachelor's degree in health sciences, life sciences, or related field preferred
• Certification as a Clinical Research Coordinator (CCRC) is an advantage
• 5+ years of experience in clinical research coordination or management
• 2+ years of experience managing medical device studies, preferably vascular access

Technical Skills and Relevant Technologies

·      Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint) and clinical trial software

·      Experience with electronic health records (EHR) systems

·      Experience with electronic data capture systems