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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.

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