Clinical Research Coordinator II Position Available In Orange, Florida
Tallo's Job Summary: The Clinical Research Coordinator II position involves recruiting, screening, and assessing patient eligibility for research studies and trials. This role requires coordinating patient care, bio-specimen collection, and informed consent processes across multiple locations. Responsibilities also include ensuring regulatory compliance, providing patient interactions during trials, maintaining HIPAA-protected databases, developing research protocols, managing budgets, and implementing SOPs for the research division. Qualifications include neurology therapeutic experience, a Bachelor's degree with 2 years of experience or an Associate's degree with 3 years of experience, or an allied health certificate program with 4 years of experience.
Job Description
Clinical Research Coordinator II Shift:
Onsite Monday-Friday 8:00 am-4:30 pm Qualifications (Must Have): Neurology theraputic experience preferred, but any other theraputic is accepted AND one of the below Bachelor’s degree in Healthcare Administration, Research, or related field and 2 year of Clinical Research Coordinator experience OR Associates degree in Healthcare Administration, Research, or related field and 3 years of Clinical Research Coordinator experience OR Graduate of an accredited allied health certificate program with 4 years of Clinical Research Coordinator experience Clinical Research Coordinator II Recruit, screen, and assess eligibility of patients for research studies, trials, and programs. Coordinate patient care, follow-up, and bio-specimen collection (blood, tissue) with clinical staff and labs. Execute and manage informed consent processes across multiple locations, requiring travel or technology use. Ensure regulatory and protocol compliance through collaboration with clinical research staff and departments. Provide concierge-level service for patient interactions during clinical trials. Maintain HIPAA-protected databases linking patient info to bio-specimens; perform chart reviews and data collection. Assist in developing compliant research protocols and control documents. Serve as the point of contact for participants, investigators, and research staff. Implement SOPs for the research division and ensure compliance with clinical research standards. Conserve hospital resources while managing project budgets from various funding sources.
