Contract Research Assistant
Behavioral Health Market Context
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Qualifications
- •High School diploma required
- •Prior clinical research, laboratory, and phlebotomy experience required
- •Ability to work independently, manage time effectively, and maintain high attention to detail required
- •The contractor is not eligible for Circuit Clinical's employee benefits
- •Work is performed on a per-assignment basis according to operational and study needs
- •2 more items(s)
Responsibilities
- •Circuit Clinical is seeking a Contract Research Assistant to support clinical trial operations by assisting Research Coordinators with study protocol visits and related operational tasks
- •The Research Assistant will provide services on an as-needed basis while maintaining autonomy over how services are performed
- •The Research Assistant will collaborate closely with Research Coordinators and the Clinical Operations team and will report operationally to the VP, Site Operations for study-related coordination
- •The Contract Research Assistant will support the execution of clinical research studies by performing delegated clinical and operational tasks in accordance with study protocols, institutional policies, sponsor requirements and applicable regulatory standards
- •Conducting study procedures, as directed by the Research Coordinators, including: measuring vital signs, performing ECGs, phlebotomy and sample collection
- •Collecting, processing, storing, and shipping laboratory specimens per protocol
- •Generating and maintaining accurate laboratory and study-related logs
- •Preparing for study visit by gathering source and essential documents, preparing lab kits, and securing required materials
- •Accurately documenting visit data in electronic data capture systems
- •Supporting participant recruitment efforts, including contacting and screening potentially eligible participants
- •The contractor is responsible for their own taxes, insurance, and business expenses unless otherwise specified
- •8 more items(s)
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