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Associate Specialist, Regulatory Affairs - Hybrid

Merck • Rahway, NJ, US • published 2026-09-25 05:23:59.568518

Description

Job Description This role will work within Global Regulatory Affairs in the Health Registration Management (HRM) Business Process Operations group to help with the continued transition and daily business operations of HRM and Veeva Registrations. The role will support our business system global userbase and release of marketed and clinical product, compliance reporting, and submissions to the HA. This role will be involved in creating, updating, and implementing process documentation, training materials, education resources, reporting and metrics, and data governance. This role will provide direct support to collaboration teams and workshop facilitators to enable capture of all future requirements needed for successful continued support of evolving business needs and keeping pace with regulatory requirements. The objective of this role will be to ensure a smooth transition for our users to the system platform by providing support cross functionally. The role will also support lifecycle management, including change control process enablement. This candidate should excel at consistent collaboration enabling cross functional critical business partnerships ensuring compliance to align ...

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