Global Regulatory & Site Activation Specialist
Listed on 2026-09-28
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Healthcare
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Research/Development
Worldwide Clinical Trials seeks a Regulatory Affairs professional in the United States to support global submissions and country-specific labeling. You will coordinate plan, organize and file regulatory submissions, and liaise with translation teams and country authorities to ensure compliance.
The role requires a four-year science degree and at least three years in clinical research, with experience in regulatory submissions and ICH GCP guidance.
Are you ready to take on the Global Regulatory & Site Activation Specialist role at Worldwide Clinical Trials?
Full responsibilities and requirements are described in the listing above.
Learn more about the Global Regulatory & Site Activation Specialist role in the description above.
We appreciate your interest in this position.
Join Worldwide Clinical Trials and contribute to our ongoing work.
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