Strategic Regulatory Study Start-Up Specialist
CTI Clinical Trial and Consulting Services, Inc.
CTI Clinical Trial and Consulting Services, Inc. is seeking a Regulatory Affairs Study Start Up Specialist (level dependent on experience) to manage essential regulatory documentation for global clinical studies and to support timely submissions to IRBs, ECs, and Competent Authorities. You’ll interact with study teams, sites, sponsors and CTI management to collect, review, reconcile, and archive documentation, perform QC checks, adapt informed consent forms, and provide ongoing status updates. #J-18808-Ljbffr CTI Clinical Trial and Consulting Services, Inc.
Vacancy posted 3 days ago
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