All jobs → Partner boards
Associate Specialist - Regulatory Affairs (Hybrid)
Merck • Philadelphia, PA, US • published 2026-10-08 21:03:19.981168
Apply on source siteDescription
Job Description The Associate Specialist of Regulatory Planning \& Publishing works closely with various stakeholders of regulatory and safety submissions to assist in activities related to planning, execution, and management of delivery of high quality and timely regulatory submissions. This position is based at the Philadelphia, PA, WeWork Office, on a hybrid bases\- 3 days in office; The incumbents will be required to commute to the Philadelphia, PA, WeWork Office, for these 3 days. The responsibilities of the incumbent may include the following: * Maintain accountability for use of established planning and tracking practices and systems. * Participate in pilots for new tools and processes. * Collaborate with colleagues inside and outside of the department, as appropriate. * Participate in training courses to increase job role skills and regulatory knowledge. **Program:** * Support in the creation of FDA cover letters and forms, creation of submission plans, assist in tracking deliverable timelines of components, and archiving in systems. **Shared Services:** (Regulatory Submission Specialist) * Provide regulatory submission/systems support. * Manage regulatory documents, assist...
Get jobs like this daily in Telegram: @careeri_bot