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A global biopharmaceutical firm is seeking a Manager for Clinical Trial Transparency Registries & Redaction. This role involves overseeing clinical study registrations and creating redacted documents for regulatory submissions. The ideal candidate should possess a Bachelors degree in life sciences, outstanding communication skills, and experience with Adobe Acrobat software. Attention to detail and the ability to manage multiple tasks are essential for success. This position is based in Warsaw, Poland and supports compliance with EU and FDA regulations.
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