Clinical Research Nurse ! Allergy & Immunology Research Phoenix Q
Listed on 2025-12-27
-
Healthcare
Clinical Research -
Research/Development
Clinical Research
Location:
Phoenix
Shift: Mon‑Fri, Days, 8am‑5pm
Category:
Research
Posting #: 987415
Employee Type:
Full-Time
This position provides and coordinates clinical care for research subjects. It has a central role in assuring participant safety, ongoing maintenance of informed consent, integrity of protocol implementation, and accuracy of data collection, data recording and follow‑up. It also engages in study procedures including administration of investigational drugs, detailed clinical assessments including adverse event assessments, and performing laboratory tests. Additional nursing care may be necessitated by the response of the participant to the study intervention.
The position is responsible for study coordination and data management, with a central focus on managing subject recruitment and enrollment, consistency of study implementation, data management and integrity, and compliance with regulatory and institutional requirements and reporting. It will support the Principal Investigator and Research team for departmental studies under minimal supervision.
- Provides nursing care to research study patients, including:
- Performs and/or schedules medical tests within the scope of nursing licensure, including laboratory tests, vital sign readings, imaging studies, cardiac and/or pulmonary function tests, and psychological evaluations.
- Administers study medications and performs patient assessments during clinic visits to determine presence of side effects; notifies the principal investigator and responds to findings/issues.
- Provides patient education and medical information to study patients and their families to ensure understanding of proper medication dosage, administration and disease treatment.
- Documents medical data in patient chart to ensure availability of timely records for decision making.
- Ensures assigned studies are conducted in accordance with FDA, OHRP, and GCP guidelines, including:
- Reviews all regulatory requirements to ensure implementation of appropriate methods, practices, and procedures for all research activities in designated area.
- Responsible for the completion and submission of documents to the appropriate IRB and institutional committees on an ongoing basis.
- Maintains compliance with current and accurate documentation in the regulatory binders as required by regulations and sponsors.
- With the principal investigator, explains the study purpose, parameters, and requirements of the studies to the participants.
- Coordinates research subject informed consent and entry into appropriate research studies ensuring that all inclusion and exclusion criteria are met.
- Coordinates the process for opening new studies, including:
- Obtains needed background material(s) on proposed research projects; presents findings and information to attending physician/principal investigator.
- Completes feasibility questionnaires.
- Circulates the confidentiality disclosure and trial agreements to the appropriate parties.
- Creates study budgets and works with management to determine financial feasibility and resources necessary to conduct the trial.
- Develops workflow procedures for study team based on specific protocol.
- Completes all tasks required by study sponsors, including:
- Provides regulatory documents to sponsor in a timely manner.
- Completes case report forms, data entry, and maintains source documentation for all study participants.
- Tracks and reports adverse events per sponsor and institutional guidelines.
- Coordinates research monitor visits and responds to all data queries.
- Participates in recruitment and selection of study participants; coordinates and participates in research subject informed consent and entry into appropriate research studies ensuring that all inclusion and exclusion criteria are met.
- Reviews monthly financial reports, including study participant billing, expenditures, and revenue. Maintains inventory level of all supplies and equipment, initiates requisitions for replacement items, and maintains equipment to provide for continuous operational efficiency.
- Participates in a variety of professional development programs to ensure ongoing awareness and understanding of most current…
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