SharePoint Maintenance Activities; Support GRT member transition by setting up transition form
Liaise cross-functionally to generate periodic internal milestone report
Performs simple analyses as directed
Support planning and managing timely deliverable of critical regulatory deliverables (registration samples) and various Module 1 documents for ex-US,ex-EU countries
Request certificates from respective Health Authority (FDA, EMA, Swiss Medic) and manage notification process
Shipping of documents, as required
Admin- scanning, copying, shipping label
Product Divestiture: Upload relevant documents into the Virtual Data Room (VDR) for potential buyers
Product Deletions: Gather information from the Country Regulatory Managers for Product Deletions Strategy
Tracks deletion notifcations to country Reg HA
Asset Integration: Upload incoming documents to the BMS systems, ensure correct update of meta data; Remediation of documents, as directed
Schedule RRT meetings and communicate timelines
Set up response templates to ensure submission readiness
Submission of responses for publishing
Support preparation of GRS analytics and monthly dashboards, eg submission, Approvals, key achievements, miles stones
Qualification & Experience
Minimum of a Bachelor degree in a Natural Science, Pharmacy, or other Healthcare-related field