Overview: Looking to be part of something more meaningful? At HonorHealth, you’ll be part of a team, creating a multi-dimensional care experience for our patients.
You’ll have opportunities to make a difference.
From our Ambassador Movement to our robust training and development programs, you can select where and how you want to make an impact.
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HonorHealth is one of Arizona’s largest nonprofit healthcare systems, serving a population of five million people in the greater Phoenix metropolitan area.
The comprehensive network encompasses six acute-care hospitals, an extensive medical group with primary, specialty and urgent care services, a cancer care network, outpatient surgery centers, clinical research, medical education, a foundation, an accountable care organization, community services and more.
With nearly 14,000 team members, 3,700 affiliated providers and hundreds of volunteers dedicated to providing high quality care, HonorHealth strives to go beyond the expectations of a traditional healthcare system to improve the health and well-being of communities across Arizona.
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Qualifications: Education
High School Diploma or GED Required
Responsibilities: Job Summary
Position provides support for clinical trials and activities in the maintenance of clinical research at HonorHealth Research Institute.
The position works closely with Research Coordination, Regulatory, and trial administration Staff to manage administrative activities, data management, and archiving activities as assigned.
They will help transition paper records to online electronic binders in accordance with FDA Regulations, International Council of Harmonization, and Good Clinical Practices and manage the collection and distribution of performance metrics
Provides data management project support for clinical research trials in an activation stage and active stage, including patient pre-screening for study eligibility, support for data submission and records clinical information in case report forms.
Assists in the coordination and management of the CTMS to ensure trial activities are documented correctly and the finance team can bill promptly.
Assists with subject follow-up for assigned clinical protocols.
Supports record archiving of documentation no longer needed for trial management, scans paper-based binders and converts to electronic binders as assigned.
Support the collection of data points for HRI2 processes and distribute to program management and HRI2 leadership for review and performance analysis
Maintains clear and regular communication with the Research Staff regarding project updates and assignments made.
Provides input and assistance to the Research Staff in maintaining the Regulatory Binders for all ongoing research studies in accordance with FDA regulations and sponsor requirements.
.
Maintains working relationships with external customers (e.
g.
professional research organizations and physicians) to facilitate the submission of clinical investigational material to the appropriate regulating body.
Performs other related duties as assigned.
Facility: Shea Medical Center Department: HHRI Data Coordination Work Hours: 8-5 Shift: 01 - Days Position Type: Regular Full-Time
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