Contract: Permanent Full Time Closing Date: 05/12/25 We are seeking Global Regulatory Affairs Specialists to provide critical subject matter expertise and backfill internal SMEs during a major regulatory transformation initiative. These roles will ensure continuity of day to day regulatory…
Contract: Permanent Full Time Closing Date: 05/12/25 We are seeking Regulatory Business Analysts to support our ongoing Veeva RIMS implementation. This role serves as the critical link between regulatory business teams and the technical implementation team, ensuring requirements are accurately…
Contract: Permanent Full Time Closing Date: 05/12/25 We are looking for Senior Regulatory Data Analysts/Data Quality Specialists to support one of the most critical workstreams in our Veeva RIMS implementation: cleansing, standardizing, and preparing legacy regulatory data for migration. If…
Contract: Permanent Full Time Closing Date: 05/12/25 We are seeking a Regulatory Data Quality Analyst to support critical data remediation and migration activities as part of our RIMS implementation. This role ensures regulatory data integrity, compliance, and alignment with business…
Contract: Permanent Full Time Closing Date: 05/12/25 We are seeking Senior Regulatory Submissions Managers to play a pivotal role in shaping how regulatory submissions are managed within our new Veeva RIMS platform. This is a high impact opportunity to influence…
Contract: Permanent Full Time Closing Date: 05/12/25 We are seekingRegulatory Process Design Managers/PMO Leads to drive the redesign of future state (“to be”) regulatory processes as part of our Veeva RIMS transformation program. This role is ideal for someone who…
Contract: Permanent Full Time Closing Date: 05/12/25 We are seeking a Senior Regulatory Data Migration Lead to oversee the end to end migration of regulatory data and documents into Veeva Vault RIM. This high impact role ensures data integrity, compliance,…
Contract: Permanent Full Time Closing Date: 05/12/25 We are seeking a Global Regulatory Data Standards Expert to lead the implementation and governance of ISO IDMP standards and ensure ongoing compliance with EMA requirements for structured medicinal product data. This role…