At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. We ensure the highest-quality review of data and effective interaction with study sites, including on-site monitoring throughout a study, ensuring that patients receive needed care, as well as identifying and treating clinical trial participants.
Performs PPD clinical research services investigator file reviews and logging of outstanding issues in project related tracking tools
Reviews regulatory documents for proper content
Disseminates study related information, including project tracking updates to Clients, clinical study teams and other PPD clinical research services departments
May assist the project team with the preparation of regulatory compliance review packages
Responsible for adhering to Good Clinical Practices, country specific regulations, PPD clinical research services /Client Standard Operating Procedures and Working Practice Documents regulations for all non-clinical/clinical aspects of project implementation, execution, and closeout
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
Outstanding communication, teamwork, interpersonal and time management skills
Excellent German (C1 level) and English languages
Schwerbehinderte Bewerber werden bei gleicher Eignung bevorzugt behandelt.