1. Performs investigator file reviews and logging of outstanding issues in project related tracking tools
2. Reviews regulatory documents for proper content
3. Liaises with monitor and investigative sites to resolve outstanding regulatory issues identified
4. Disseminates study related information, including project tracking updates to Clients, clinical study teams and other PPD departments
5. Assists with the identification of potential investigators and development/distribution of initial protocol packets
6. Creates meeting agendas and minutes, as well as coordinates team conference calls and distribution of meeting minutes
Requirements
7. University degree, or equivalent in education, training and experience
8. Ability to effectively analyse project specific data/systems to ensure accuracy and efficiency
9. Experience of manage multiple projects with differing priorities at one given time
10. Exceptional communication, collaboration, organisational and time management skills
11. Fluency in Spanish and English is essential
Why Thermo Fisher Scientific?
At Thermo Fisher Scientific, you will work with a team that values integrity, intensity, innovation, and involvement. Our collaborative environment empowers you to excel and compete at the highest levels. Join us, and together we will successfully implement solutions that make a difference in the world!