Elevate your career as a Clinical Trial Assistant I with Everest, focusing on operational excellence and compliance in clinical trials. Collaborate with diverse stakeholders to manage trial documentation and support regulatory submissions.
In this entry-level role, you will handle administrative tasks that ensure compliance with ICH-GCP and local regulations. Your responsibilities will include maintaining essential trial documents, assisting in regulatory submissions, and contributing to clinical operations documentation. This position suits candidates with strong communication skills and familiarity with electronic Trial Master Files.
Key Responsibilities:
• Interact with study sponsors and vendors for trial operations
• Compile and review documentation for clinical site qualifications
• Assist in the preparation of regulatory documents
• Set up and maintain study archives in TMF and CTMS
• Track monitoring compliance metrics and issue reminders
Requirements: