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Role Overview:
- This position provides operational and systems support for DaVita Clinical Research by executing day-to-day Clinical Trial Management System (CTMS) workflows.
- You will support clinical research teams, investigators, and site personnel to ensure smooth trial operations across multiple studies.
Key Responsibilities:
- Manage the setup, configuration, and maintenance of CTMS study builds while translating protocols into actionable system configurations.
- Execute month-end clinical trial activities, including subject visit approvals and stipend card operations.
- Provide frontline end-user support, conduct data audits, and escalate complex technical issues to senior team members.
Qualification Highlights:
- BS/BA in science, statistics, or a related field is required.
- Experience with Tableau, research databases (e.g., RAVE, Medidata), or CTMS is strongly preferred.
- Intermediate to advanced proficiency in Microsoft Excel and Office 365 Suite is required.
What DaVita Provides:
- Comprehensive benefits including medical, dental, vision, and 401(k) match.
- Paid time off, PTO cash out, and family support resources such as backup child/elder care.
- Professional development programs and on-demand virtual leadership courses through DaVita's StarLearning platform.
DaVita Clinical Research
DaVita Clinical Research is a specialized arm of DaVita, a comprehensive kidney care provider focused on transforming care and improving quality of life for patients globally. The company serves more than 200,000 patients across 2,800+ dialysis centers in the U.S. and operates in 11 other countries, with a culture centered on community, belonging, and clinical innovation.