Worldwide Clinical Trials in Mexico City is seeking a TMF Operations professional. The role includes processing and reviewing Trial Master File documents, preparing quality control checklists, and ensuring adherence to regulatory standards. Candidates should have 1-2 years of experience in the CRO/Pharma industry and possess strong data collection and communication skills. Proficiency in Microsoft Word and Excel is required, with a preference for a university degree in Life Sciences. Join a global team committed to improving lives and fostering an inclusive environment.
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