About this opportunity
CTI lists this Global Regulatory Start-Up Lead opportunity in covington, North Carolina. Review the employer’s description below for duties, qualifications and application requirements.
Job description
CTI Clinical Trial and Consulting Services in Covington, NC seeks a Regulatory Documentation Specialist to manage essential regulatory documentation for global clinical studies and coordinate submissions with IRBs, ECs, and authorities.
You will review study documents, ensure compliance by country requirements, assist project teams, and maintain TMF and submission packages across sites.
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Who can apply
Review the original listing for work authorization, qualifications and employer requirements.