Bilingual Clinical Research Coordinator II (Bilingual-English & Spanish) Position Available In Orange, Florida
Tallo's Job Summary: The Bilingual Clinical Research Coordinator II position requires fluency in both English and Spanish, with a preference for experience in Neurology therapy. The role involves recruiting, screening, and assessing patient eligibility for research studies, coordinating patient care and bio-specimen collection, managing informed consent processes, ensuring regulatory compliance, and providing high-level patient service during clinical trials. Additionally, the coordinator will maintain databases, assist in protocol development, manage project budgets, and implement SOPs for the research division.
Job Description
Bilingual Clinical Research Coordinator II (MUST BE Bilingual-English & Spanish) Direct Hire Placement with benefits on day 1!
Shift:
Onsite Monday-Friday 8:00 am-4:30 pm MUST BE Bilingual-English & Spanish 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 Bilingual Clinical Research Coordinator II (MUST BE Bilingual-English & Spanish) 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.
