Clinical Trial Specialist

Job Summary

A company is looking for a Clinical Trial Specialist.

Key Responsibilities

• Support clinical trial activities as the in-house site start-up and maintenance specialist
• Assist with the collection of essential documents for site initiation/startup and submissions to IRBs/Ethic Committees
• Perform quality control of documents and maintain the Trial Master File (TMF) for clinical trials

Required Qualifications

• College/University diploma/degree or at least 2 years of related experience/training
• Exposure to medical terminology is preferred
• Knowledge of ICH/GCP, ethical, and regulatory requirements is preferred
• Ability to perform general administrative duties as needed