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Senior Clinical Study Manager
1 week ago
As a Clinical Research Associate II, you will be responsible for managing assigned sites from initiation through close-out. This includes building relationships with investigators and site staff, facilitating access to study systems, and ensuring compliance with project-specific training requirements.
You will also evaluate site-level data, address issues at sites, and ensure that all relevant documents are submitted to the Trial Master File (TMF). Additionally, you will participate in investigator and external meetings, audits, and regulatory inspections as required.
This is an excellent opportunity to develop your expertise in clinical research and contribute to the success of our site management team.