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Traveling Clinical Research Coordinator
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Based on Florida data
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What they do
A Clinical Research Coordinator directs clinical research and development projects for companies, and coordinates testing and quality control.
$113,064 / year median in Florida
+12% projected growth
Job Description
Job Description Help for Job Description. Opens a new window. Overview
- Coordinate clinical research activities across multiple sites, ensuring compliance with protocols and regulatory standards.
- Travel extensively to research sites, Monday through Thursday, with weekends at home.
- Collaborate with site teams to studies in compliance with GCP, FDA, and ICH guidelines.
- Screen, enroll, and follow up with patients participating in vaccine trials.
- Perform clinical procedures such as vital signs, ECGs, and phlebotomy as required.
- Document and report adverse events, deviations, and non-compliance promptly.
- Ensure proper documentation and data entry in electronic data capture systems.
- Assist in study start-up activities, including training and site initiation visits.
- Support recruitment and community outreach efforts to enhance study enrollment. Key Responsibilities & Duties
- Screen patients for eligibility and obtain informed consent for clinical trials.
- Conduct patient follow-up visits and document findings in clinical charts.
- Perform basic lab procedures, including specimen collection and processing.
- Coordinate and schedule patient visits, ensuring adherence to study protocols.
- Maintain study-specific supplies and ensure proper inventory management.
- Handle IRB functions and regulatory compliance tasks independently.
- Assist in training new research assistants and coordinators as needed.
- Resolve monitoring visit issues promptly and effectively.
- Participate in investigator meetings and community outreach events. Job Requirements
- Bachelor of Science degree required, with 3-4 years of clinical research experience.
- Proficiency in clinical procedures such as phlebotomy, ECGs, and vital signs.
- Experience in vaccine trials and managing high patient volumes is essential.
- Strong organizational, communication, and interpersonal skills are required.
- Proficiency with electronic health records and data capture systems.
- Ability to travel extensively and work onsite during weekdays.
- Knowledge of GCP, FDA, and ICH regulations and guidelines.
- Bi-lingual proficiency in English and Spanish is a plus.
- Self-motivated with a strong work ethic and professional demeanor.