The Talent Acquisition Specialist will manage full-cycle recruitment for Clinical Operations positions across the United States. They will partner with hiring managers to identify, attract, and hire top talent while maintaining accurate records in the ATS.
You will design and execute clinical studies while providing strategic regulatory guidance to help clients navigate FDA requirements. This involves creating presubmission packages, developing study protocols, and defending clinical evidence to ensure successful product approvals.
The Project Manager will lead global clinical or medical device trials by coordinating cross-functional teams and managing project timelines and milestones. They are responsible for monitoring project finances, identifying risks, and ensuring all deliverables align with study protocols.
The Statistical Programmer will own the statistical programming process, creating analysis datasets and programming tables, listings, and figures. They will interpret study protocols and ensure all outputs meet validation and quality standards in a regulated environment.
