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Associate Director, Global Regulatory Affairs @ Merck Group

Billerica, Massachusetts, United StatesOnsiteFull-timePosted 4 days ago

Opens on the employer's site

About this role

Embrace the opportunity to become an Associate Director, Global Regulatory Affairs and drive regulatory strategy for oncology programs. Lead submissions, ensure compliance, and collaborate with global teams. Shape regulatory excellence and make a real impact in drug development. Grow your career in a dynamic, cross-functional environment with opportunities for leadership and innovation.. Category: Regulatory Affairs

Skills

regulatory strategyregulatory submissionslifecycle managementcompliance managementrisk assessmentpharmacovigilancestakeholder managementoncology regulatory affairsregulatory complianceregulatory strategy developmentregulatory submissions (us/eu/irl)labeling negotiationsregulatory risk mitigationmatrix team leadershipregulatory agency interaction

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