Clinical Research Ops Analyst II — Data & Process Improvement

University of Texas; Austin (TX); On-site; USD 54,935 - 67,142; Full time

Job summary

University of Texas in Austin seeks a Clinical Research Operations Analyst II to support the lifecycle of clinical trials by delivering operational analyses, dashboards, and workflow optimization across centralized services.

You will coordinate CTMS and Epic Research workflows, assist with study start-up and regulatory activities, and drive efficiency and compliance through standardized processes and actionable metrics.

Qualifications

• Bachelor’s degree and 2+ years in clinical research operations.
• Experience with CTMS, Epic Research, or related research systems.
• Knowledge of GCP and FDA-regulated clinical research preferred.

Responsibilities

• Support operational coordination across centralized clinical research services including study start-up and regulatory support.
• Develop operational dashboards and performance reports for activation timelines and enrollment.
• Coordinate workflows across Epic Research, CTMS, and electronic regulatory systems.
• Lead process improvements to reduce activation timelines and improve efficiency.
• Collaborate with research administration, regulatory affairs, and clinical operations.

Skills

Operational analytics

Performance reporting

Research systems support

Clinical trial operations

Education

Bachelor’s degree in Healthcare Administration, Public Health, Life Sciences, Business Administration, or related field

Tools

CTMS

Epic Research

Electronic regulatory platforms

Job description

University of Texas in Austin seeks a Clinical Research Operations Analyst II to support the lifecycle of clinical trials by delivering operational analyses, dashboards, and workflow optimization across centralized services.

You will coordinate CTMS and Epic Research workflows, assist with study start-up and regulatory activities, and drive efficiency and compliance through standardized processes and actionable metrics.