Role OverviewThe Clinical Research Specialist 1 will identify, develop, and implement process development and process improvement solutions to optimize global trial workflow timelines. They will develop and execute device processes associated with clinical trials, ensuring compliance with regulations and managing the lifecycle of devices.
What You Will Do
The successful candidate will coordinate procurement of study inventory, manage shipment of devices to clinical sites, confirm receipt of study product, and track product through to final disposition. They will also generate transparency reporting data and reports to support Sunshine Act compliance.
Why It Might Be a Fit
The ideal candidate will have 2 years of clinical research experience and an Associate's/Bachelor's degree in a related field. They will be able to support clinical research laboratory operations as needed and perform other incidental duties as assigned.
Requirements
- 2 years of clinical research experience
- Associate's/Bachelor's degree in a related field
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