Senior Regulatory Start-Up Specialist — Global Trials
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CTI Clinical Trial and Consulting Services is seeking an experienced Regulatory Affairs professional to support Study Start-Up (RASSU) activities across multiple countries. You will advise project teams on regulatory requirements and oversee submissions to IRBs/ECs, ensuring quality and compliance across sites.
Responsibilities include adapting study documents, coordinating with site personnel, and maintaining regulatory packages per sponsor SOPs.
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