Applications Systems Analyst ((CTMS) Portfolio: OnCore and eReg) - ITS-Research Information Sys

Galveston, TX, US • Posted 9 hours ago • Updated 9 hours ago
Full Time
On-site
Fitment

Dice Job Match Score™

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Job Details

Skills

  • Computer Science
  • Health Informatics
  • Good Clinical Practice
  • HIPAA
  • SQL
  • Data Extraction
  • Reporting
  • Workflow
  • Information Systems
  • Clinical Trials
  • Clinical Trial Management System
  • Clinical Research
  • Management
  • Research
  • Information Technology
  • Documentation
  • Preventive Maintenance
  • Project Management
  • Performance Management
  • SAP BASIS
  • Law

Summary

Minimum Qualifications:

Bachelor's degree equivalent and one (1) year of related experience.

Preferred Qualifications:
  • Bachelor's degree in computer science, health informatics, information systems, or a related field.
  • Hands-on experience administering or supporting a clinical trial management system, electronic regulatory binder platform, electronic data capture system, or comparable research application.
  • Working knowledge of clinical research operations, including protocol lifecycle, subject enrollment, IRB submission and approval workflows, and study documentation requirements.
  • Familiarity with regulatory frameworks governing clinical research systems, including 21 CFR Part 11 electronic records and signatures, Good Clinical Practice, and HIPAA.
  • Ability to write SQL queries or build reports for data extraction and operational reporting.

Job Summary:

Under general direction, this position is responsible for providing basic to intermediate analysis and documentation of business and management problems for systems and programming requirements. Assist in providing solutions to problems utilizing more efficient operational procedures, workflows, and information technology solutions.

Job Duties:
  • Within ITS-Research Information Systems, this position serves as the primary technical administrator for the institution's clinical trial management system (CTMS) portfolio: OnCore and eReg.
  • The analyst partners daily with the Office of Clinical Research, study coordinators, and research administration to configure protocols, manage user access, maintain regulatory binder structures, resolve system issues, and act as the day-to-day liaison to the software vendor.
  • The role sits at the intersection of research operations and information technology, and it supports systems that carry regulated study documentation subject to institutional, sponsor, and federal oversight.

Salary Range:

Actual salary commensurate with experience.

Work Schedule:

Remote position. 8 am to 5 pm, and as needed on occasion.

Equal Employment Opportunity

UTMB Health strives to provide equal opportunity employment without regard to race, color, religion, age, national origin, sex, gender, sexual orientation, gender identity/expression, genetic information, disability, veteran status, or any other basis protected by institutional policy or by federal, state or local laws unless such distinction is required by law. As a Federal Contractor, UTMB Health takes affirmative action to hire and advance protected veterans and individuals with disabilities.
Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.
  • Dice Id: 10156302
  • Position Id: ec0ff74271ee56a371a21fbd1f619fd5
  • Posted 9 hours ago
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