Centralized Clinical Research Operations Analyst II Full-time NEW

Centralized Clinical Research Operations Analyst II

Dell Medical School is seeking a Centralized Clinical Research Operations Analyst II. This is a grant-funded position with an end date of September 30th, 2029, renewable based on availability of funding, work performance, and progress toward goals.

The Centralized Clinical Research Operations Analyst II supports advanced operational activities within the Clinical Trials Office (CTO). This position leads operational analysis, performance reporting, workflow optimization, and research systems coordination that support the clinical trial lifecycle across centralized clinical research services. Working under the direction of the Manager, Clinical Research Operations, this role supports development and implementation of standardized operational processes, performance dashboards, and research technology integrations that enable efficient and compliant clinical trial operations. The Analyst II provides operational insights, manages operational improvement initiatives, and supports cross-functional coordination across research administration, regulatory affairs, research finance, and clinical operations. This role contributes to the development of scalable operational infrastructure that supports growth of the institutional clinical research enterprise.

Responsibilities include:

• Clinical Research Operations Analysis & Program Support
• Operational Reporting, Data Analytics & Performance Monitoring
• Research Systems Integration & Operational Technology Support
• Process Improvement & Workflow Optimization
• Cross-Functional Operational Coordination
• Marginal or Periodic Functions

Knowledge, skills, and abilities required include:

• Integrity and Trust
• Process Management
• Managing and Measuring Work
• Problem Solving
• Customer Focus
• Communicating Effectively
• Dealing with Ambiguity

Education and experience requirements include:

• Minimum Qualifications:
• Bachelor's degree in Healthcare Administration, Public Health, Life Sciences, Business Administration, or related field.
• 2 years of experience in clinical research operations, research administration, program coordination, research systems support, or related healthcare operations roles.
• Experience supporting clinical trial operational workflows including study start-up, regulatory coordination, research coordination services, or research program administration.
• Experience working with research technology systems such as Clinical Trial Management Systems (CTMS), electronic regulatory platforms, or electronic health record research modules.
• Preferred Qualifications:
• Experience supporting operational analytics, performance reporting, or research program management within an academic medical center.
• Experience supporting research system implementations or research operational infrastructure development.
• Knowledge of Good Clinical Practice (GCP), human subjects research regulations, and FDA-regulated clinical research environments.

Salary range: $61,039+ depending on qualifications

Working environment/equipment includes:

• Standard office equipment
• Repetitive use of a keyboard
• Occasional interaction with clinical research staff in clinical environments

Required materials include:

• Resume/CV
• 3 work references with their contact information; at least one reference should be from a supervisor
• Letter of interest