Clin/Tran Research Coord II (Sleep Tech)

Key Responsibilities

• Coordinate the approval processes and conduct of sleep research protocols from start-up through close-out
• Manage IRB/regulatory activities (submissions, amendments, continuing review, documentation)
• Conduct and support 1–2 NIH-funded/federally sponsored sleep studies each week
• Ensure protocol adherence, accurate documentation, and high-quality data collection
• Partner with investigators, clinical staff, and research support teams to keep studies running smoothly and on timeline

Technical Capabilities

• Study Design & Conduct (Novice): Applies qualitative and quantitative research methods to perform preparatory, regulatory, and analytic tasking within the life cycle of a study.
• Project Coordination (Novice): Reviews specific project related documents for completeness and accuracy and ensures project status reports are received, when due, from project managers for all approved projects.
• Communication (Novice): Clearly, effectively and respectfully communicates to employees or customers.

Breadth of Knowledge

• Has developed networking skills which assist in researching issues.
• Knows what information is available in the company.
• Designs data collection forms.

Core Capabilities

• Serving Others with Compassion: Seeks to understand current and future needs of relevant stakeholders and customizes services to better address them.
• Solving Complex Problems: Approaches problems from different angles; Identifies new possibilities to interpret opportunities and develop concrete solutions.
• Offering Meaningful Advice and Support: Provides ongoing support and coaching in a constructive manner to increase employees' effectiveness.