Clinical Research Nurse 2

Full-Time Clinical Research Nurse 2The University of Miami/UHealth Department of SCCC CRS has an exciting opportunity for a Full-Time Clinical Research Nurse 2 to work at UHealth in Miami, Florida.The Clinical Research Nurse 2 ensures the integrity and quality of clinical research studies are maintained and conducted in accordance with practice guidelines, federal and sponsor regulations, and institutional policies and procedures. Additionally, the Clinical Research Nurse 2 plays a key role in the recruitment of participants and achievement of research objectives.Core job functions include:Assessing, troubleshooting, and reporting problems with data collection to appropriate managing staff.Identifying desired research outcomes and evaluating and monitoring subjects' responses.Conducting initiation visits and registering patients in clinical studies.Performing study data collection and entry using charts, correspondence, medical records, and relevant communications.Educating staff and subjects about protocols, treatment, possible side effects, and complications.Preparing and processing new research proposals and amendments and continually monitoring applications and adverse events.Assisting with study completion, data lock, study closeout, and archiving of study files to ensure completeness and continuity of all study data.Completing ongoing checks of clinical data entered on the case report forms to ensure accuracy and revising any discrepancies.Adhering to University and unit-level policies and procedures and safeguarding University assets.Core qualifications include:Bachelor of Science in nursing required. Graduated from an accredited nursing program.Current Florida Registered Nurse license; Current American Heart Association (AHA) Basic Life Support (BLS) for healthcare providers Certification Oncology Nursing Society (ONS) provider card for Chemotherapy and Immunotherapy administration.Certification in a relevant specialty or field (i.e., oncology, diabetes, clinical research, etc.) preferred.Minimum of 3 years of relevant experience.Strong, effective communication skills with patients, families, and clinical team for innovative patient care and trust.Ability to collaborate with peers in the best interest of the patient to provide consistent quality of care.Ability to establish and maintain positive, caring relationships with executives, managers, physicians, non-physician providers, patients/families and other departments and staff.Ability to adapt and exhibit flexibility to handle new, different, or changing environments.Demonstrates strong time management skills to prioritize, triage, and act proactivity.Ability to uphold professional ethics and maintain patient confidentiality.Knowledgeable on all aspects of patient care including assessing, planning, coordinating, monitoring, and evaluating the patients' progress through continuum of care.Knowledge in navigating the electronic medical records and reviewing treatment plans.Skill in completing assignments accurately and with attention to detail.Ability to work evenings, nights, and weekends as necessary.Commitment to the University's core values.Ability to work independently and/or in a collaborative environment.Critical thinking, analytical and problem-solving abilities required as related to various aspects of the protocol.Good reading, writing, mathematical, organizational and comprehension skills.Demonstrate ability to maintain cooperative working relationships with internal and external units in a clinical research environment.