Clinical Trial Coordinator - Segrate, Milan

at  Thermo Fisher Scientific

EDUCATION AND EXPERIENCE:

• Master’s degree (ideally within a clinical specialism), or equivalent education, training and experience
• Experience with Submissions to Ethics Committees and Regulatory bodies (desired)
• Ability to effectively analyse project specific data/systems to ensure accuracy and efficiency
• Experience of manage multiple projects with differing priorities at one given time
• Exceptional communication, collaboration, organisational and time management skills

• Performs PPD investigator file reviews and logging of outstanding issues in project related tracking tools
• Reviews regulatory documents for proper content
• Liaises with monitor and investigative sites to resolve outstanding regulatory issues identified
• Disseminates study related information, including project tracking updates to clients, clinical study teams and other PPD departments
• Responsible for adhering to Good Clinical Practices, country specific regulations, PPD/Client Standard Operating Procedures and Working Practice Documents regulations for all non-clinical/clinical aspects of project implementation, execution, and closeout
• Assists with the identification of potential investigators and development/distribution of initial protocol packets
• Creates meeting agendas and minutes, as well as coordinates team conference calls and distribution of meeting minute