As part of our continued commitment to providing a safe and healthy workplace, Phoenix Children’s is officially a mandatory COVID-19 vaccination organization, effective October 1, 2021. All new employees must be fully vaccinated prior to starting employment at Phoenix Children’s. Having a vaccinated workforce is an important step in supporting our mission to provide hope, healing and the best healthcare for the children in our community.

Positions at Phoenix Children's

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Work in an environment focused on passion, teamwork and continuous learning with a career at Phoenix Children's.

Biostatistics Intern

The Biostatistics Intern is mentored by a professional PhD Biostatistician to gain statistical consulting experience and develop skills required to provide statistical services for clinical research and quality studies. Specific tasks include literature review, protocol development, sample size calculations, data cleaning, statistical analyses for various data types using the statistical software R, results summary, interpretation of statistical estimates, and contributing to abstract and manuscript writing. The Biostatistics Intern may be included as a co-author on conference presentations and publication.

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Clinical Research Assistant

This position assists in the coordination of various research projects and supports the Principal Investigator and other Clinical Research support staff in the acquisition of specimens and extraction of data from patient charts. This position also provides administrative/regulatory support by assisting with patient recruitment; scheduling study participants; providing operational support for the implementation and delivery of research studies; maintaining complete and accurate data and source documentation; and processing IRB and other regulatory documents as needed in accordance with federal, state, and regulatory agency and local requirements.

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Clinical Research Assistant

This position assists in the coordination of various research projects and supports the Principal Investigator and other Clinical Research support staff in the acquisition of specimens and extraction of data from patient charts. This position also provides administrative/regulatory support by assisting with patient recruitment; scheduling study participants; providing operational support for the implementation and delivery of research studies; maintaining complete and accurate data and source documentation; and processing IRB and other regulatory documents as needed in accordance with federal, state, and regulatory agency and local requirements.

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Clinical Research Coordinator

This position is responsible for the coordination of a variety of research projects from pre-study implementation through study closure and will work independently in the acquisition of specimens; extraction and entry of patient data; maintenance of complete and accurate subject data and regulatory documentation; and analysis of data per protocol. This position provides administrative / regulatory support (recruiting, interviewing and scheduling study participants, processing IRB and other regulatory documents) to specific clinical departments in accordance with all federal, state, regulatory agency, and specific institutional requirements.

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Clinical Research Coordinator

This position is responsible for the coordination of a variety of research projects from pre-study implementation through study closure and will work independently in the acquisition of specimens; extraction and entry of patient data; maintenance of complete and accurate subject data and regulatory documentation; and analysis of data per protocol. This position provides administrative / regulatory support (recruiting, interviewing and scheduling study participants, processing IRB and other regulatory documents) to specific clinical departments in accordance with all federal, state, regulatory agency, and specific institutional requirements.

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Clinical Research Coordinator

This position is responsible for the coordination of a variety of research projects from pre-study implementation through study closure and will work independently in the acquisition of specimens; extraction and entry of patient data; maintenance of complete and accurate subject data and regulatory documentation; and analysis of data per protocol. This position provides administrative / regulatory support (recruiting, interviewing and scheduling study participants, processing IRB and other regulatory documents) to specific clinical departments in accordance with all federal, state, regulatory agency, and specific institutional requirements.

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Clinical Research Intern

The Clinical Research Intern is responsible for learning the basics of a clinical research trial. The goal of the internship is to introduce the student to the concepts of, the lifecycle of, and the execution of clinical trials in medicine. The Clinical Research Intern carries out needed tasks as part of ongoing and future clinical research projects within the designated department. This position is assigned a mentor and works directly with a research team in all aspects of conducting research. The focus of research is determined by the department and this position functions as a supportive role while learning various aspects of conducting clinical trials.

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Clinical Research Nurse

This position provides and coordinates clinical care for research subjects. This position 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. This position 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. This 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. This position will support the Principal Investigator and Research team for departmental studies under minimal supervision.

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Clinical Research Nurse

This position provides and coordinates clinical care for research subjects. This position 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. This position 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. This 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. This position will support the Principal Investigator and Research team for departmental studies under minimal supervision.

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Clinical Research Nurse - Gastro Research Studies

This position provides and coordinates clinical care for research subjects. This position 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. This position 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. This 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. This position will support the Principal Investigator and Research team for departmental studies under minimal supervision.

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Clinical Trials Regulatory Coord

The Scientist participates in the development and writing of investigator-initiated clinical cancer trials and be the primary individual responsible for submission of these protocols (and their reports/renewals and related correspondence) to regulatory agencies (such as the US FDA). In addition, the Scientist oversees the performance and analyses of ancillary biological studies to achieve the scientific aims of those clinical trials, analyze collected lab and clinical data and serve as a co-investigator/co-author for publications related to these clinical trials. The overall aim of the clinical research initiatives in the Division of Pediatric Hematology, Oncology, and Bone Marrow Transplant (The Division) is to improve outcomes for children with cancer and non-malignant hematologic diseases.

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Research Assistant

This position assists in the coordination of various research projects and supports the Principal Investigator and other Clinical Research support staff in the acquisition of specimens and extraction of data from patient charts. This position also provides administrative/regulatory support by assisting with patient recruitment; scheduling study participants; providing operational support for the implementation and delivery of research studies; maintaining complete and accurate data and source documentation; and processing IRB and other regulatory documents as needed in accordance with federal, state, and regulatory agency and local requirements.

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Scientific Research Writer

The Scientific Research Writer is a key member of the Research team responsible for providing high-level guidance and support to researchers on scientific writing and grantsmanship expertise in all phases of the research writing process, including assistance in coordination and preparation of grants, concept papers, and manuscripts. The Scientific Research Writer specializes in substantive scientific and technical editing, stylistic and content editing, rewriting, formatting, editing and proofreading manuscripts for publication, internal and external grant proposals and study protocols. This includes critical review of the text for clarity, persuasiveness and comprehensive presentation. The primary emphasis of the writer is on reading, reviewing, analyzing and providing theoretical guidance for grant proposals and original manuscripts for scientists and clinicians.

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