What Youll Do: Conduct pre-entry review of clinical data Review and issue queries for case report form (CRF) data based on automated edit checks, manual review, and sponsor requirements Assist with set-up of data management study files and the collection,
What Youll Do: Assist in organizing, composing, and producing professional letters, summaries, reports, minutes, etc, using Microsoft Office software including Word, Access, and Excel Proofread documents ensuring grammar, spelling, and punctuation are correct Assist in developing
Please submit your application and CV in English What Youll Do: Plan, implement, evaluate, and complete full execution of assigned clinical trials; often functions as a global trial lead. Set goals, and timelines, provide oversight and