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Clinical Research Coordinator

United States of America, Baton Rouge · Job Posted March 21, 2026
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Job Description

Works under the supervision of the Principal Investigator (PI), Director and other site personnel. Conceptually applies the research protocol to the clinical setting. Maintains appropriate documentation. Ensures studies are conducted according to company policies and applicable regulations.

Job Responsibility

  • Develops in-depth understanding of each study protocol to ensure all aspects of the protocol are adhered to
  • Under supervision prepares and submits regulatory documents
  • In collaboration with the PI, identifies potential study participants
  • Obtains informed consent
  • Schedules subject visits
  • Prepares labs/tests per protocol
  • Responsible for study drug storage and drug accountability
  • Administers the investigational product
  • Monitors and evaluates patients’ condition
  • Consults with PI regarding administration of investigational product
  • Conducts routine assessments
  • Educates the subject about the study
  • Documents subject information
  • Meets with the study monitor to review data
  • Reviews all lab/tests with the physician
  • Reports subject’s progress, complaints and issues
  • Conducts ongoing assessments of the overall study execution
  • Notifies appropriate management of serious adverse events
  • Collects pre-study essential documents
  • Maintains the study file record
  • Maintains subject participant records
  • Provides a list of all study participants to management
  • Ensures appropriate storage of records pertaining to investigational product
  • Documents investigational product received dispensed, and returned
  • Completes clinical trials management system and case report forms
  • Attends Investigator Meetings

Requirements

  • Bachelor’s Degree or an equivalent combination of education and experience
  • Graduate of a technical program in healthcare (e.g. LVN/LPN, Medical Assistant or Dialysis Technician) AA in Life Sciences or other health related field
  • 2 to 5 years’ healthcare experience with Dialysis experience preferred
  • Research experience preferred
  • Willing to pursue CCRC or SoCRA certification when eligible
  • Current appropriate state licensure if applicable
  • Proficient with PCs and Microsoft Office applications
  • Good communication and organizational skills
  • Ability to work independently

Nice to have

  • Dialysis experience preferred
  • Research experience preferred
  • Advanced Degree preferred

What we offer

  • Healthcare
  • Continuing Education
  • Paid Time Off
  • Collaborative Environment
  • Additional Perks
  • 401(k) Retirement Saving

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