Worldwide Clinical Trials is seeking an Associate II, TMF Operations for a remote European-based role. You will review, process, and quality-check TMF documentation across complex studies, ensuring ALCOA principles and ICH GCP standards are met.You will collaborate with general teams, prepare QC checklists, and maintain study documentation while supporting RMC Leads and SharePoint activities. English proficiency and attention to detail are essential.#J-18808-Ljbffr