Senior Site Management Associate
Job Summary
Serving as the main site contact for non-trial-participant issues, the full-time Senior Site Management Associate will manage records flow, prepare regulatory documents, and coordinate site payments while working remotely.
Key responsibilities
- Manage records flow with sites and off-site facilities, ensuring compliance with regulatory requirements
- Coordinate payments to sites and prepare for site audits and inspections
- Provide training and support to investigator site teams and oversee the preparation of Investigator Site Files
Required qualifications
- College or university degree or equivalent combination of education, training, and experience
- Minimum 3 years of experience in the clinical research industry, preferably in a similar role
- 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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