Position Details

Salary $57K – $85K USD / year

Type Not Specified

Experience entry

Exp. Years Minimum 1 year of clinical research experience managing studies from start up to close out

Education High School Diploma or equivalent is required. Bachelor's Degree is preferred.

Category Science & Research

About this role

Coordinate and execute late-phase nephrology clinical research trials at DaVita Clinical Research sites. Own study execution from enrollment through close out while ensuring protocol compliance and accurate data management to support database lock.

Key Responsibilities

Execute clinical trials through all phase of the study: enrollment, maintenance and close out
Perform research procedures according to the study protocol and coordinate with the physician investigator
Serve as liaison between physicians, sponsors, and facility teammates
Deliver or exceed enrollment targets
Enter data accurately in electronic data entry systems and resolve data queries to meet database lock timelines

Technical Overview

Manage clinical trial operations including GCP-compliant research procedures per study protocol. Perform accurate and timely data entry into electronic data entry systems and resolve data queries ahead of database lock, while coordinating closely with Principal Investigators, sponsors, and site teams.

Ideal Candidate

The ideal candidate is an entry-level Clinical Research Coordinator with at least 1 year of clinical research experience coordinating studies from start up through close out. They are strong in GCP (Good Clinical Practice), executing study protocol procedures, maintaining accurate and timely electronic data entry, and resolving data queries before database lock. They can collaborate effectively with physicians (Principal Investigator/Sub-Investigator), sponsors, and facility teammates in a dialysis-nephrology setting.

Must-Have Skills

clinical research experience managing studies from start up to close out or equivalentgood clinical practice (GCP)study protocol executionaccurate and timely data entrytimely resolution of data queriescompliance with applicable healthcare and research regulationsadherence to DaVita Clinical Research standard operating procedures and policies

Nice-to-Have Skills

experience in nephrology clinical research trialsexperience coordinating late phase clinical trials

Tools & Platforms

electronic data entry systems

Required Skills

coordinationmanagement and conduct of nephrology clinical research trialsenrollmentmaintenance and close outresearch proceduresstudy protocolPrincipal InvestigatorSub-Investigatordata entryelectronic data entry systemsdata queriesdatabase lockGood Clinical Practice (GCP)compliancestandard operating procedureshealthcare regulationsresearch regulationsliaison

Hard Skills

clinical trialslate phase clinical trialsenrollmentmaintenance and close outresearch proceduresstudy protocoldata entryelectronic data entry systemsdata queriesdatabase lockgood clinical practice (GCP)complianceDCR standard operating procedures and policieshealthcare regulationsresearch regulationsliaison between Principal Investigator and sponsorsnephrology clinical researchGCP compliancedata query resolution

Soft Skills

collaborationcommunicationrelationship buildingaccountabilitycompassionproblem solvingteam ownership of resultsliaison skills

Industry & Role

Industry Healthcare

Job Function Coordinate and manage nephrology clinical research trials with GCP-compliant operations and accurate clinical data management.

Role Subtype Clinical Research Coordinator

Keywords for Your Resume

Clinical Research CoordinatorClinical Research Study Coordinatornephrology clinical research trialsdialysis centersphysicians practicesclinical trialslate phase clinical trialsenrollmentmaintenance and close outresearch proceduresstudy protocolPrincipal InvestigatorSub-Investigatorstudy sponsorsDaVita facility teammatesdata entryelectronic data entry systemsdata queriesdatabase lockGood Clinical Practice (GCP)GCPcompliancestandard operating proceduresDCR standard operating proceduresapplicable healthcare and research regulationstimely resolutionreliable transportation to travel between sites

Deal Breakers

High School Diploma or equivalent is required, Minimum 1 year of clinical research experience managing studies from start up to close out or equivalent experience, Ability to travel between study sites (reliable transportation to travel between ... is required)

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