Clinical Research Coordinator

Full Time @Davita posted 6 months ago

Job Description

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.

The Clinical Research Study Coordinator (Research Coordinator) serves to lead in the coordination, management and conduct of nephrology clinical research trials in dialysis centers and physicians practices. DaVita Clinical Research (DCR) is a Renal Research site network conducting clinical trials across the country. 


  • Accountable for the successful execution of clinical trials through all phase of the study: enrollment, maintenance and close out.
  • Responsible for performing research procedures according to the study protocol and working in partnership with the physician investigator to coordinate research activities.
  • Serves as a liaison between the physicians (Principal Investigator or Sub-Investigator), study sponsors and DaVita facility teammates.
  • Responsible to deliver or exceed project enrollment targets for clinical research studies at their site.
  • Responsible for accurate and timely data entry into the electronic data entry systems.
  • Responsible for timely resolution of all data queries to meet project timelines for database lock.
  • Demonstrates compliance with good clinical practice (GCP) and applicable law, and verifies that study teams comply with GCP and applicable law.
  • Demonstrates adherence to DCR standard operating procedures and policies and with the standards customary in the clinical research industry.
  • Understands and promotes compliance with all applicable healthcare and research regulations.


  • Bachelor’s degree or equivalent experience required. Minimum 2 years of experience as a clinical research coordinator is strongly preferred.  Must have experience with late phase drug and device trials (phase 2, 3, 4).
  • 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.
  • 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
  • Travel required up to 10% depending on business needs.
  • Experience in managing confidential information and/or issues using discretion and judgment.

Here is what you can expect when you join our Village:
• A “community first, company second” culture based on Core Values that really matter.
• Clinical outcomes consistently ranked above the national average.
• Award-winning education and training across multiple career paths to help you reach your potential.
• Performance-based rewards based on stellar individual and team contributions.
• A comprehensive benefits package designed to enhance your health, your financial well-being and your future.
• Dedication, above all, to caring for patients suffering from chronic kidney failure across the nation.

Join us as we pursue our vision “To Build the Greatest Healthcare Community the World has Ever Seen.”
Why wait? Explore a career with DaVita today.
Go to to learn more or apply.

Join us as we pursue our vision “To Build the Greatest Healthcare Community the World has Ever Seen.”

Why wait? Explore a career with DaVita today.

Go to to learn more or apply.

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