At DaVita Clinical Research (DCR), a contract research organization, a wholly owned subsidiary of DaVita Inc., we use our extensive, applied database and real-world healthcare experience to assist pharmaceutical and medical device companies in the design, recruitment and completion of retrospective, prospective and pragmatic clinical trials. <?xml:namespace prefix = "o" />
DCR’s scientific and clinical expertise spans the lifecycle of product development with more than 175 client companies over the last 30+ years.
Unlike most contract research organizations, we are part of an integrated company that provides healthcare.
This unique structure enables us to integrate real-world experience and de-identified data with our operational excellence, superior customer service, and flexibility. From clinical trial design and execution to health outcomes research and publication planning, we offer a range of services to help with your project, regardless of where it is in the product life cycle.
The Data Entry Coordinator is responsible for the creation and maintenance of study data collection tools (eg, source documents) to ensure complete and accurate collection of required clinical research study data.
ESSENTIAL DUTIES AND RESPONSIBILITIES:
DaVita is an equal opportunity/affirmative action employer. As such, DaVita makes hiring decisions solely on the basis of qualifications and experience, and without regard to age, race, color, religion, sex, gender identity, sexual orientation, national origin, disability or protected veteran status.