Clinical Project Coordinator

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