Skip to Main Content

Job Title


Coordinator Research - Lab AdminGeneral


Company : Christus Health


Location : Corpus Christi, TX


Created : 2026-04-19


Job Type : Full Time


Job Description

CHRISTUS Spohn Hospital Corpus Christi - Shoreline overlooking Corpus Christi Bay is the largest and foremost acute care 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