Project Management Specialist

Job Summary

Supporting the successful performance of clinical trials, the fully remote Project Management Specialist will manage project tasks, coordinate regulatory document submissions, and facilitate communication between departments from study award to closure.

Key responsibilities

• Perform set-up, maintenance, and closeout of project files and study information on relevant systems
• Track milestone progress in real time, providing rationale for delays and assisting with contingency plans
• Prepare regulatory documents for IRB approvals and oversee ongoing submissions and amendments

Required qualifications

• BS/BA in Life Science or related discipline
• Minimum of one year of clinical research experience or experience in a healthcare setting
• Previous GCP training and certification preferred
• Experience with electronic medical records and clinical trial management systems
• Strong computer skills, including proficiency in MS Office products