Senior Site Management Associate
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Job Summary
Managing site-related issues and vendor communications, the full-time Senior Site Management Associate will serve as the main contact for non-trial participant matters while coordinating regulatory submissions and site audits in a remote work environment.
Key responsibilities
- Act as the primary site contact for vendor and trial supply management, addressing non-protocol related issues
- Prepare and manage regulatory submissions, ethics committee documents, and coordinate site payments
- Organize site audits, monitor EDC completion progress, and provide training for investigator site teams
Required qualifications
- College or university degree or equivalent experience in clinical research
- Minimum 3 years of experience in the clinical research industry, preferably with a CRO
- Basic proficiency in MS Word, Excel, Outlook, and PowerPoint
- Knowledge of applicable software and project-specific systems following proper training
Complete Job Description
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