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Clinical Research Admin Support
4 months ago
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.
Join us. Let’s go beyond expectations and transform healthcare together.
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.
- 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
