Clinical Research Coordinator – DCR

DaVita Kidney Care

. Coordinate, manage, and conduct nephrology clinical research trials in dialysis centers and physician practices .

Posted 10/6/2026full-timeHenderson • Nevada • United StatesJuniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in managing nephrology clinical research trials, ensuring compliance with GCP and healthcare regulations while effectively coordinating with physician investigators and study sponsors. Proficient in data entry and project management to meet enrollment targets and maintain study integrity.

Highest-signal resume keywords

Clinical Research ExperienceGood Clinical Practice (GCP)Certified Clinical Research Coordinator (SOCRA or ACRP)Data Entry AccuracyProject Management

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Research ManagementData EntryResearch Procedure ExecutionStudy Protocol AdherenceEnrollment Target Achievement

Soft Skills

InitiativeTime ManagementDiscretion and JudgmentAdaptabilityCommunication

Tools & Technologies

Electronic Data Entry Systems

Certifications & Qualifications

Certified Clinical Research Coordinator (SOCRA or ACRP)

Industry Keywords

NephrologyClinical TrialsHealthcare RegulationsResearch ComplianceStandard Operating Procedures

About the role

Key responsibilities & impact

Coordinate, manage, and conduct nephrology clinical research trials in dialysis centers and physician practices
Coordinate and execute all aspects of late-phase clinical trials in the Henderson and surrounding areas
Execute clinical trials through enrollment, maintenance, and closeout
Perform research procedures according to study protocols
Partner with physician investigators to coordinate research activities
Serve as liaison between physicians, study sponsors, and DaVita facility teammates
Deliver or exceed project enrollment targets
Enter data accurately and timely into electronic data entry systems
Resolve data queries promptly to meet project timelines for database lock
Demonstrate compliance with GCP and applicable laws
Verify study-team compliance with GCP and applicable laws
Adhere to DCR standard operating procedures, policies, and clinical research industry standards
Promote compliance with healthcare and research regulations

Requirements

What you’ll need

High School Diploma or equivalent is required
Bachelor's Degree is preferred
Minimum 1 year of clinical research experience managing studies from start up to close out or equivalent experience
Reliable transportation to travel between local research sites
Commitment to and role model of DaVita’s values
Ability to manage multiple projects, meet deadlines, and adjust priorities in an evolving work environment
Self-starter with a high degree of initiative, urgency, and follow-through
Experience managing confidential information and/or issues using discretion and judgment
Certified Clinical Research Coordinator (SOCRA or ACRP) preferred
Knowledge of good clinical practice (GCP) and applicable healthcare and research regulations
Ability to perform research procedures according to study protocols
Ability to enter data accurately and promptly into electronic data entry systems

Benefits

Comp & perks

Flexible weekly work schedule based on current business needs
December Industry wellness break (week between Christmas and New Year’s Day)
Medical, dental, and vision coverage
401(k) match
Paid time off
PTO cash out
Family resources
EAP counseling sessions
Access to Headspace®
Backup child and elder care
Maternity/paternity leave
Professional development programs
On-demand virtual leadership and development courses through StarLearning
Performance-based rewards
Award-winning education and training
Comprehensive benefits package
Competitive total rewards package