On-Site Clinical Research Systems Analyst

Oklahoma-State-University; Oklahoma; On-site; USD 65,000 - 85,000; Full time

Job summary

The OSU Center for Health Sciences in Oklahoma seeks a Clinical Research Systems Analyst to support, maintain, and optimize CTMS, eRegulatory, eSource, and related applications across the study lifecycle.

You will work with clinical operations, IT, regulatory affairs, and compliance to ensure systems are validated, access-controlled, audit-ready, and aligned with GCP and 21 CFR Part 11.

Qualifications

• Bachelor's degree or higher in a health science, information systems, computer science, or related field.
• 2–5 years of experience in clinical research operations, research informatics, or system administration.
• Experience with CTMS, eReg, eSource, or EDC systems.
• Understanding of GCP, Part 11, and data integrity principles.

Responsibilities

• Support, maintain, and optimize computerized systems used in clinical research.
• Ensure systems are configured to support compliant operations and validated.
• Partner with clinical operations, IT, regulatory affairs, compliance, and quality teams.
• Maintain data integrity and audit-ready configurations across the study lifecycle.

Skills

Analytical thinking

Problem solving

Operational requirements to system

Communication and training

Documentation accuracy

Education

Bachelor's degree in health sciences, information systems, computer science, or related field

Tools

CTMS

eRegulatory

eSource

EDC

Job description

The OSU Center for Health Sciences in Oklahoma seeks a Clinical Research Systems Analyst to support, maintain, and optimize CTMS, eRegulatory, eSource, and related applications across the study lifecycle.

You will work with clinical operations, IT, regulatory affairs, and compliance to ensure systems are validated, access-controlled, audit-ready, and aligned with GCP and 21 CFR Part 11.