EMEA Regulatory Affairs Manager — Remote

Company: Worldwide Clinical Trials
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Job Description:

Worldwide seeks a senior Regulatory Affairs professional to lead global submissions across EMEA, APAC and LATAM, ensuring compliance with evolving regulations. The role involves coordinating ethics submissions, supporting business development, and mentoring junior staff in a fast-paced, multinational environment.

The candidate will provide expert regulatory advice, prepare technical documents like IMPDs and IBs, and liaise with sponsors, project managers, CRAs and Medical & Scientific Affairs

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Posted: September 25th, 2026