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DaVita·Las Vegas, NV

Clinical Research Coordinator (DCR)

Healthcare AdministrationFull time
iPosting details
ScheduleFull time
EducationHS diploma/GED · Bachelor's degree preferred
Experience1+ years
SourceDaVita · posted Oct 6, 2026
✓Requirements
Certifications
Certified Clinical Research Coordinator (SOCRA or ACRP) – preferred
Education
✓High School Diploma or equivalent is required.
Bachelor's Degree is preferred.
Qualifications
✓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 with ability to demonstrate those positively and proactively to patients, teammates, management, physicians, and/or vendors (Village Service Partners) in everyday performance and interactions.
✓Ability to manage multiple projects, meet deadlines, and adjust priorities appropriately in an evolving work environment with shifting time frames; self-starter with high degree of initiative, urgency, and follow through.
✓Experience in managing confidential information and/or issues using discretion and Judgment
✓DaVita Clinical Research (DCR), a wholly owned subsidiary of DaVita Inc., is the research arm of DaVita.
✓DCR innovates through retrospective outcomes research aimed at improving care and quality of life for people with kidney disease.
✓DCR assists pharmaceutical and medical device companies in the design, recruitment and completion of clinical trials using its renal research site network.
✓For 30 years we have helped 500+ clients with their development projects.
✓DCR is based in Minneapolis, MN and operates in locations across the US.
+Benefits
✓Medical, dental and vision
✓401(k) with match
✓Paid time off
✓Wellness and mental health resources
✓Continuing education
+DaVita
9administration roles open
Las VegasNV
Pay for this position
Pay not listed
Apply to DaVitaContact Recruiter about this role
✓You’ll need
Certifications
Certified Clinical Research Coordinator (SOCRA or ACRP) – preferred
Education
✓High School Diploma or equivalent is required.
Bachelor's Degree is preferred.
Qualifications
✓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 with ability to demonstrate those positively and proactively to patients, teammates, management, physicians, and/or vendors (Village Service Partners) in everyday performance and interactions.
✓Ability to manage multiple projects, meet deadlines, and adjust priorities appropriately in an evolving work environment with shifting time frames; self-starter with high degree of initiative, urgency, and follow through.
✓Experience in managing confidential information and/or issues using discretion and Judgment
✓DaVita Clinical Research (DCR), a wholly owned subsidiary of DaVita Inc., is the research arm of DaVita.
✓DCR innovates through retrospective outcomes research aimed at improving care and quality of life for people with kidney disease.
✓DCR assists pharmaceutical and medical device companies in the design, recruitment and completion of clinical trials using its renal research site network.
✓For 30 years we have helped 500+ clients with their development projects.
✓DCR is based in Minneapolis, MN and operates in locations across the US.
+Benefits
Medical, dental and vision401(k) with matchPaid time offWellness and mental health resources

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About the role

Accountable for the successful execution of clinical trials through all phase of the study: enrollment, maintenance and close out.

What you’ll do
Accountable for the successfulAccountable for the successful execution of clinical trials through all phase of the study: enrollment, maintenance and close out
Responsible for performing researchResponsible for performing research procedures according to the study protocol and working in partnership with the physician investigator to coordinate research activities
Responsible to deliver orResponsible to deliver or exceed project enrollment targets for clinical research studies at their site
Responsible for accurate andResponsible for accurate and timely data entry into the electronic data entry systems
Responsible for timely resolutionResponsible for timely resolution of all data queries to meet project timelines for database lock