Clinical Research Coordinator (DCR)

DAVITA•Las Vegas, NV

31d•Onsite

About The Position

DaVita Clinical Research is seeking a motivated, positive, and innovative Clinical Research Coordinator to coordinate, manage, and conduct nephrology clinical research trials in dialysis centers and physician practices. The role is based at the Las Vegas, Nevada site and coordinates and executes all aspects of late-phase clinical trials in Las Vegas and surrounding areas. A flexible weekly work schedule may be available based on business needs. The coordinator is accountable for study execution from enrollment through maintenance and closeout, performs protocol-required research procedures in partnership with physician investigators, and coordinates with physicians, sponsors, and DaVita facility teammates. The role also supports enrollment targets, accurate and timely electronic data entry, timely data-query resolution, and compliance with good clinical practice, applicable laws, DCR procedures, policies, and healthcare and research regulations.

Requirements

High school diploma or equivalent.
At least 1 year of clinical research experience managing studies from start-up through closeout, or equivalent experience.
Reliable transportation to travel between local research sites.
Commitment to and ability to model DaVita’s values in interactions with patients, teammates, management, physicians, and vendors.
Ability to manage multiple projects, meet deadlines, and adjust priorities in an evolving work environment with shifting time frames.
Self-starter with initiative, urgency, and follow-through.
Experience managing confidential information or issues with discretion and judgment.

Nice To Haves

Bachelor’s degree.
Certified Clinical Research Coordinator certification through SOCRA or ACRP.

Responsibilities

Coordinate, manage, and conduct nephrology clinical research trials in dialysis centers and physician practices.
Execute clinical trials through all study phases, including enrollment, maintenance, and closeout.
Perform research procedures according to study protocols and partner with physician investigators to coordinate research activities.
Serve as a liaison among physicians (Principal Investigators or Sub-Investigators), study sponsors, and DaVita facility teammates.
Meet or exceed clinical research study enrollment targets at the site.
Enter study data accurately and on time into electronic data-entry systems.
Resolve data queries promptly to meet project timelines for database lock.
Demonstrate compliance with good clinical practice (GCP) and applicable law, and verify study-team compliance.
Follow DCR standard operating procedures and policies and customary clinical research industry standards.
Understand and promote compliance with applicable healthcare and research regulations.

Benefits

Medical insurance.
Dental insurance.
Vision insurance.
401(k) match.
Paid time off, including PTO cash out.
December industry wellness break during the week between Christmas and New Year’s Day.
Family resources and EAP counseling sessions.
Access to Headspace.
Backup child and elder care.
Maternity and paternity leave.
Professional development programs and on-demand virtual leadership and development courses through StarLearning.
Flexible weekly work schedule, based on current business needs.
Performance-based rewards.
Education and training across multiple career paths.