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Coordinator Research - Lab AdminGeneral

Christus Health
United States, Texas, Corpus Christi
600 Elizabeth Street (Show on map)
Apr 10, 2026
Description

CHRISTUS Spohn Hospital Corpus Christi - Shoreline overlooking Corpus Christi Bay is the largest and foremost acutecare medical facility in the region, with a full range of diagnostic and surgical specialty services in cardiac, cancer, and stroke care. It is the leading emergency facility in the area with a Level II Trauma Center in the Coastal Bend, staffed with physicians and nurses specially trained in emergency services.

  • The Pavilion and North Tower house a state-of-the-art emergency department, ICU, Cardiac Cath Lab, and surgical suites
  • A teaching facility in affiliation with the Texas A&M University System Health and Science Center College of Medicine
  • Accredited Chest Pain Center
  • Accredited Joint Commission Stroke Team

Summary:

The Research Coordinator provides administrative and fiscal support for the department. Specific responsibilities include, but are not limited to: maintaining all administrative functions of the office and researching and preparing grant applications that support institutional research.

Responsibilities:


  • Maintains consistency with Administrative and Departmental policies with appropriate behavior, dress, attitude, attendance, confidentiality, professionalism, and reliability.
  • Implements established procedures to process application packets (applications for review, research protocols, and consent forms).
  • Maintains official records of the committee's activities and preparation of meeting materials, assuring that applications are complete and accurate prior to committee review.
  • Prepare and distribute IRB packets, prepare IRB agenda, and minutes.
  • Prepare and maintain IRB member files and IRB study files.
  • Compose meeting result letters to study investigators, relaying specific Board requests and timely follow-up of the same.
  • Implement IRB internal Quality Assurance (QA) process for compliance with OHRP/FDA regulations and internal standard operating procedures.
  • Coordinate and process all IRB Safety Reporting.
  • Maintain and continually refine a customized, networked computerized database to allow for the timely tracking of research projects scheduled for re-review.
  • Research, write, and coordinate the submission of grant proposals to support research.
  • Prepare reports as required.
  • Other duties as assigned.

Requirements:


  • Associate's Degree in Nursing required

Work Schedule:

8AM - 5PM Monday-Friday

Work Type:

Full Time


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