Bilingual Clinical Research Coordinator II (LOCATED In Orlando,FL) Position Available In Miami-Dade, Florida
Tallo's Job Summary: Bilingual Clinical Research Coordinator II (LOCATED in Orlando, FL) requires relocation to Orlando, FL area. Direct hire with benefits. Must be bilingual in English & Spanish. Responsible for patient recruitment, screening, and coordinating care for research studies. Bachelor's degree with 2 years of experience, or Associates degree with 3 years, or allied health certificate with 4 years. Manages informed consent processes, ensures regulatory compliance, and provides concierge-level service to patients. Maintains HIPAA-protected databases and assists in protocol development. Point of contact for participants, investigators, and research staff. Implement SOPs and manage project budgets.
Job Description
Bilingual Clinical Research Coordinator II ( LOCATED in Orlando, FL) MUST be able to relocate on your own to the Orlando, FL area (no relocation offered) 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) MUST be able to relocate on your own to the Orlando, FL area (no relocation offered) 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.
