Clinical Project Coordinator

Job Summary

To support clinical studies, the full-time Clinical Project Coordinator will manage study details in CTMS and GoClinical, serve as the primary contact for site communications, and oversee logistics for decentralized visits while working remotely with potential hybrid office collaboration.

Key responsibilities

• Create and maintain study details in CTMS and GoClinical, including all related contact information and visit tracking
• Coordinate day-to-day communications with sites, manage document submissions, and oversee logistics for shipping and tracking
• Assist the GCPM with study document creation, training materials, and site setup activities, including audits and study closeout tasks

Required qualifications

• Bachelor's degree or equivalent experience with a minimum of 3 years in a related field
• At least 2 years of experience in clinical study, research, or healthcare
• Current knowledge of ICH/GCP and applicable regulations
• Proficiency in Microsoft Office and Adobe Acrobat applications
• Ability to work independently and collaboratively in a team environment