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

Posting Note: Must be a Local candidate and be able to work on-site.

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 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 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 Trials Compliance Analyst

This position is responsible for conducting comprehensive research audits and monitoring of clinical trials to ensure faculty, staff, employees and students engaged in research activities are compliant with all aspects of federal, state and local policies and regulations governing clinical research. This position reviews internal regulatory documentation, protocols, amendments, correspondence, case report forms, study data, research billing reports, and adverse event reports. This position also determines overall protocol compliance which includes review of the consent process and eligibility criteria. Medical records, laboratory data, and other source documentation is utilized to examine study data accuracy and completeness. This position prepares audit and monitoring reports based on findings, works with research management to create corrective and preventative action plans, and assists in the development of education and training with respect to the conduct of clinical trials. The Clinical Trials Compliance Analyst is an integral member of the Office of Research. Under the direction of the Director, Research Operations, the Clinical Trials Compliance Analyst promotes and facilitates a culture of compliance through audit activities designed to identify risk and support adherence with Federal, State, and Local Regulations and Guidelines. This includes but is not limited to providing educational programming and tools to facilitate compliant research, conduct quality assurance reviews of data to support reporting and working with the research community to establish standards. The Clinical Trials Compliance Analyst works closely with the Manager of Clinical Research to develop quality/compliance training programs and assists with the delivery of training programs.

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Contracts Specialist-Research

Posting Note: Hybrid Position, 3 days in office, 2 days remote.

This position facilitates research contract development, legal review and negotiation for the organization. The Research Contracts Specialist, in coordination with the Office of General Counsel and Clinical Research, supports the development and implementation of research contract management tools and processes to assist in achieving the organization’s research contracting objectives and strategies. The Research Contract Specialist assumes most of the administrative and legal processing of research contracts, subject to attorney oversight as needed and per established contract guidelines. This position receives oversight from and reports to the Research Office Leadership and the Office of General Counsel. This position does not supervise any positions.

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Scientific Research Writer

Posting Note: This position is a Hybrid and requires you to work on- site at our Main Campus in Phoenix. Preferred Clinical experience.

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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