
Clinical Research Coordinator II
- Orlando, FL
- $64,480-70,720 per year
- Permanent
- Full-time
- Execute and coordinate the informed consent process for research participants across multiple locations, which may involve traveling between sites or using technology.
- Screen patients, assess eligibility, and coordinate the participation and follow-up of volunteers in research studies.
- Recruit and consent research participants for therapeutic areas served.
- Provide concierge-level service for all patient interactions during clinical trials and research studies.
- Coordinate or perform biospecimen collection (e.g., blood, tissue) and maintain HIPAA-compliant databases connecting patient information to biospecimens used in research.
- Collaborate with Clinical Research nursing staff, Research Services, laboratory teams, and hospital departments to ensure regulatory and protocol compliance.
- Work with assistant clinical coordinators to ensure compliant data entry into registries, patient records, and research-specific database systems.
- Assist Principal Investigators and research staff in developing compliant research protocols and control documents.
- Serve as the study-specific point of contact for participants, investigators, research staff, hospital departments, and external research partners.
- Collaborate with clinical research supervisors and staff to implement standard operating procedures (SOP) for the research division.
- Maintain sensitivity to cost containment measures while overseeing proposed project budgets from internal and external funding sources.
- Ability to work independently in a fast-paced clinical or research environment, handling multiple tasks effectively and timely.
- Knowledge of HIPAA data protection and patient advocacy, or similar awareness of ethical treatment of research participants.
- Effective communication skills with research participants, investigators, staff, and external partners.
- Analytical problem-solving skills with sound judgment.
- Adaptability to respond to changing needs in clinical research units.
- Proficiency in Microsoft Office applications, including Word, Excel, Access, Outlook, and Internet use.
- Bachelor’s degree in Healthcare Administration, Research, or related field with no experience required.
- Associate's degree in Healthcare Administration, Research, or related field with two years of experience.
- Graduate of an accredited allied health certificate program with four years of clinical research or healthcare experience.