Senior Manager, Regulatory Affairs

ICON · Mechelen, Belgium +5 more

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RegulatoryFull-timeCompany career page

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Role summary

Senior Manager overseeing regulatory affairs delivery and team coaching at a global clinical research organization. Responsibilities include providing regulatory expertise in drug development, preparing submission strategies, advising clients, and driving business development across multiple therapeutic areas.

Where this listing comes from

This listing was compiled by RoleLantern from the employer's publicly available posting on Workday, captured and rephrased by RoleLantern using automated (AI) tools on 2026-10-02 (originally posted 2026-10-02). It was not submitted or confirmed by the employer through RoleLantern. Details may be inaccurate, incomplete, outdated, or no longer available; please confirm with the employer's official posting before applying.

What they're looking for

Bachelor's degree in relevant scientific or healthcare discipline
Minimum 7 years regulatory affairs experience with supervisory background
Pharmaceutical or CRO industry experience (6+ years for certain regions)
Demonstrated expertise in regulatory strategies, marketing authorization applications, and agency interactions
Strong organizational and written/verbal communication skills
Management capability and attention to detail in complex environments

What you'll be doing

Oversee regulatory affairs delivery and coach team members on quality standards
Provide regulatory expertise in multi-area strategic drug development initiatives
Develop and prepare strategic development and submission plans for clients
Represent regulatory affairs in business development and identify new opportunities
Advise ICON clients on regulatory strategy across portfolio and contribute to specialized areas

Privacy & handoff

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What RoleLantern checked

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Date posted1 day ago

Last source check1 day ago

Salary listedNeeds clarity

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