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Life-Changing Research Opportunities
2 semanas atrás
Clinical Research Associates in this role will be responsible for conducting site visits, completing site visit deliverables with quality and within timelines, and adhering to regulatory requirements and SOPs.
They will assist with study start-up activities, including feasibility, pre-study activities, and site selection. They will also collect, review, and track essential documents and participate in investigator, client, and project team meetings.
The Clinical Research Associate II will create and implement subject enrollment strategies for assigned sites, ensure proper storage and dispensation of Investigational Product (IP), and perform site management activities. They will also conduct remote monitoring and utilize systems to track subject status, CRF retrieval/SDV, and IP.
This role requires the ability to identify site issues and implement corrective actions or escalate as necessary. The Clinical Research Associate II will work closely with Clinical Data Management for data cleaning activities and assist in preparing and coordinating investigator and client meetings.
Additional Key Responsibilities:
- Assist with project-specific activities as a member of the Project Team
- Support in development of CRFs and other study documents
- Support translation and review of patient information sheets and informed consent forms