Senior DMC Project Coordinator

Role Overview: You will be responsible for coordinating and supporting activities for Data Monitoring Committees (DMCs) at Fortrea. This includes tasks such as timeline generation, selection of DMC members, coordination of DMC contracts, charter development, travel arrangements, meeting organization, meeting attendance, meeting minutes, and expense reporting. Additionally, you will monitor project status to ensure all DMC deliverables and deadlines are met, while also ensuring compliance with project budget and developing DMC tracking tools and reports. You will act as a liaison between the sponsor, DMC, and internal project team, providing guidance and mentoring to less experienced DMC project coordinators. Key Responsibilities: - Coordinate and support activities for Data Monitoring Committees (DMCs) - Monitor project status to ensure DMC deliverables and deadlines are met - Develop DMC tracking tools and reports - Act as a liaison between sponsor, DMC, and internal project team - Provide guidance and mentoring to less experienced DMC project coordinators - Maintain project-specific documentation, including Study Master Files - Perform quality control of certain DMC deliverables - Ensure high-quality work delivery to internal and external clients - Organize storage and archiving of project documentation - Adhere to Fortrea SOPs, Quality Management System, and Good Clinical Practice (GCP) standards - Build and maintain good working relationships within Clinical Development Services - Interact with professionalism and discretion - Perform any other duties as needed or assigned Qualifications Required: - Bachelor's degree or higher in a health-related field - Relevant and equivalent experience may be considered in lieu of educational requirements Additional Company Details: Fortrea values individuals with a high degree of accuracy, attention to detail, teamwork, efficiency, independence, multi-tasking abilities, problem-solving skills, customer focus, written and verbal communication skills, proficiency in standard software packages, ability to work under tight deadlines, adherence to guidelines and codes of practice, knowledge of clinical trial processes, project management skills, organizational skills, business impact awareness, and a professional approach at all times. Please refer to the company's EEO & Accommodations policies for more information.,