Clinical Translational Research Coordinator III (Idrees)

Key Responsibilities

• Manages the start-up, conduct, and closeout of clinical/translational research studies focused on histotripsy.
• Ensures scientific integrity, participant safety, and full compliance with institutional policies, Good Clinical Practice (GCP), and sponsor/regulatory requirements.
• Leads day-to-day study operations such as regulatory documentation and audit readiness; accurate and timely data collection with query resolution; clinical biorepository and specimen lifecycle management (processing, inventory, multi-site tracking, and compliant shipping).
• Oversees study budgets and invoicing.
• Serves as a primary liaison among investigators, sponsors, research staff, and participants.

Technical Capabilities

• Study Design & Conduct (Intermediate): Applies qualitative and quantitative research methods to perform preparatory, regulatory, and analytic tasking within the life cycle of a study.
• Project Coordination (Intermediate): Performs project tracking and reporting relative to task completion dates, dependency effects, problem anticipation, schedule conflicts, and assignment to appropriate staff for resolution.
• Develops methods to measure customer satisfaction and obtains feedback at critical milestones and at project completion to ensure project efforts meet customer expectations.

Core Accountabilities

• Supporting Colleagues: Develops Self and Others, Builds and Maintains Relationships, Communicates Effectively.
• Ensuring High Quality: Performs Excellent Work, Ensures Continuous Improvement, Fulfills Safety and Regulatory Requirements.
• Managing Resources Effectively: Demonstrates Accountability, Stewards Organizational Resources, Makes Data Driven Decisions.
• Fostering Innovation: Generates New Ideas, Applies Technology.