Job Summary

A company is looking for a Clinical Trial Associate Site Management Associate to provide support for the execution of clinical trials.

Key Responsibilities:

• Organizes Study Team meetings and prepares meeting minutes
• Assists with organizing Investigator Meetings
• Assists with site management activities, including enrollment tracking, entries into Clinical Trial Management System, and communication with investigational sites and Clinical Research Associates

Required Qualifications:

• Bachelor's degree in life sciences discipline or relevant discipline preferred
• 2 years of relevant work experience in the biopharmaceutical industry, or the equivalent combination of education and experience
• Basic working knowledge of GCP, CFR and ICH guidelines and clinical trial operations
• Ability to work well with cross-functional Study Team and investigational sites
• Proficiency in Microsoft Office applications including Outlook, Excel, Word, and PowerPoint