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DaVita - The Woodlands, TX

posted 2 months ago

Full-time - Entry Level
The Woodlands, TX
Ambulatory Health Care Services

About the position

The Clinical Research Coordinator at DaVita Clinical Research (DCR) is responsible for leading the coordination, management, and execution of nephrology clinical research trials. This role involves working closely with physician investigators and study sponsors to ensure successful trial execution, from enrollment to closeout, while maintaining compliance with clinical research regulations and standards. The position offers a flexible work schedule and is based in Shenandoah, TX, focusing on late-phase clinical trials in the surrounding areas.

Responsibilities

  • Accountable for the successful execution of clinical trials through all phases of the study: enrollment, maintenance, and closeout.
  • Perform research procedures according to the study protocol and coordinate research activities with the physician investigator.
  • Serve as a liaison between the physicians, study sponsors, and DaVita facility teammates.
  • Deliver or exceed project enrollment targets for clinical research studies at their site.
  • Ensure accurate and timely data entry into electronic data entry systems.
  • Resolve all data queries promptly to meet project timelines for database lock.
  • Demonstrate compliance with good clinical practice (GCP) and applicable laws, ensuring study teams adhere to these standards.
  • Promote compliance with all applicable healthcare and research regulations.

Requirements

  • High School Diploma or equivalent is required; Bachelor's Degree is preferred.
  • Minimum 1 year of clinical research experience managing studies from startup to closeout or equivalent experience.
  • Reliable transportation to travel between local research sites.
  • Ability to manage multiple projects, meet deadlines, and adjust priorities in an evolving work environment.
  • Experience in managing confidential information with discretion and judgment.
  • Certified Clinical Research Coordinator (SOCRA or ACRP) is preferred.

Nice-to-haves

  • Experience in nephrology or related clinical research fields.
  • Strong communication and relationship-building skills.

Benefits

  • Flexible weekly work schedule based on business needs.
  • Comprehensive benefits including medical, dental, vision, and 401(k) match.
  • Paid time off and PTO cash out.
  • Family resources and EAP counseling sessions.
  • Access to Headspace®, backup child and elder care, maternity/paternity leave.
  • Professional development programs and online training courses.
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