Clinical Project Coordinator

Job Summary

Supporting clinical trial operations, the full-time Clinical Project Coordinator will manage diverse coordination and administrative tasks, assist with study startup and closeout activities, and ensure compliance with clinical research regulations while working remotely.

Key responsibilities:

• Coordinate and facilitate communications with investigative sites, vendors, and internal teams to support study objectives
• Maintain accurate clinical trial information and ensure the quality and compliance of Trial Master File documentation
• Assist in the development and coordination of study-specific plans and operational processes throughout the study lifecycle

Required qualifications:

• University/college degree in Life Sciences, Business Studies, or related field
• Minimum of three years of relevant coordination or administration experience in a clinical research setting
• Valid Driver's License
• Advanced proficiency in Microsoft Office Suite and various applications for reporting and data management
• Demonstrated understanding of clinical research processes and ICH-GCP guidelines