CLINICAL RESEARCH NURSE - ONCOLOGY

Toledo Clinic•Maumee, OH

1d•$30 - $40•Onsite

About The Position

The Clinical Research Nurse will ensure the integrity and quality of clinical trials are maintained and conducted in accordance with federal, state, and local regulations, Institutional Review Board (IRB) approvals, and with program Standard Operating Procedures. This position is also responsible to ensure completeness, accuracy, and compliance with each protocol and to assist Investigators of clinical studies in coordinating and facilitating the activities of study patients.

Requirements

Minimum 4 years of nursing experience in medical practice.
Proven knowledge in patient treatment and coordination of clinical care.
Experience in oncology and/or an acute care setting.
Attention to detail required in collecting and analyzing data.
Strong verbal and written communication skills for interacting with patients and reporting research findings.
DOT/IATA Training (must be obtained within 30 days of hire).
Certification in Human Subjects Protection, Good Clinical Practices (must be obtained within 30 days of hire)
Adherence to all Toledo Clinic policies and procedures.
Registered Nurse with current license to practice in the State of Ohio.

Nice To Haves

Experience conducting clinical research, including enrolling patients in research studies, implementing research protocols and presenting findings.
Knowledge of GCP.

Responsibilities

Providing nursing care to research study participants.
Ensuring compliance with each study’s protocol by providing thorough review and documentation at each subject study visit.
Participating in recruitment and selection of study participants by interviewing and documenting medical history to determine compliance with eligibility requirements.
Interfacing with study participants to support efforts to determine eligibility and consenting requirements according to protocol.
Performing medical or research required tests, including, but not limited to, vital signs, imaging studies, specimen collection and processing, and electrocardiograms.
Administering investigational medications, as applicable, and performing patient assessments during clinic visits to determine presence of side effects; notifies Principal Investigator of findings/issues.
Providing patient education and medical information to study participants to ensure understanding of proper medication dosage, administration, and disease treatment.
Documenting medical data in patient chart to capture protocol requirement.
Ensuring assigned studies are conducted in accordance with the Food and Drug Administration (FDA) and Good Clinical Practices (GCP) guidelines.
Ensuring site compliance with research protocols by reviewing all regulatory requirements to confirm implementation of appropriate methods, practices, and procedures for all research activities.
Developing accurate source materials and ensuring compliance.
Providing accurate and timely data collection, documentation, entry, and reporting in both sponsor and TCCC electronic medical record, databases / Clinical Trial Management System (CTMS), etc.
Supporting clinical research operations team in the maintenance of regulatory documents in accordance with SOP and applicable regulations.
Communicating and collaborating specific study requirements to the research team, including internal and external parties, sponsor, monitors, Investigators, and study patients.
Participating with the research operations team to identify and prioritize the development of systems and infrastructure to maintain research quality and compliance.
Maintaining good rapport and cooperative relationships.
Approaching conflict in a constructive manner.
Helping to identify problems, offer solutions, and participate in their resolution.
Maintaining the confidentiality of information acquired pertaining to patient, physicians, employees, and visitors.
Discussing patient and hospital information only among appropriate personnel.
Assuming responsibility for performance of job duties in the safest possible manner, to assure personal safety and that of coworkers, and to report all preventable hazards and unsafe practices immediately to management.
Actively demonstrating the organization's mission and core values and conducting oneself at all times in a manner consistent with these values.
Knowing and adhering to all laws and regulations pertaining to patient health, safety and medical information.