Regulatory Affairs - Regional Dossier Publisher

Merck Merck · Pharma · Central Bohemian, Czech Republic

The Regional Dossier Publisher (RDP) is responsible for publishing key regulatory submissions in the EU+EEMEA region, supporting the publishing work of the regional team. This role requires knowledge of regulatory procedures and dossier requirements, and involves supporting country RA teams with local publishing and submission transmission needs. The RDP will also assist in the development of tools and procedures for submission publishing.

What you'd actually do

  1. The RDP will be the regional expert for regulatory submission capabilities, including dossier structures and file formats, electronic submissions, and transmission (e.g., agency gateways), dossier repositories and databases.
  2. The RDP will be responsible for identifying and maintaining dossier format requirements supporting regulatory dossier assembly (aka publishing) and delivery to regulatory health authorities or to the country organization in the region.
  3. The RDP will support the maintenance of related processes in accordance with regional/country requirements and will support the central publishing team responsible for the execution of the assembly processes.
  4. The RDP will play an advocating role for standardization across the supported countries within the region.
  5. The RDP will lead technical impact assessments of regional/country requirements for regulatory submissions and serve as the technical expert for local Country RA teams and providing training to the Country RA teams on the publishing processes.

Skills

Required

  • Publishing
  • Regulatory Affairs Management
  • Drug Regulatory Affairs
  • Pharmaceutical Regulatory Affairs
  • Assembly Processes
  • Publishing Process
  • Process Management
  • Document Management
  • Electronic Document Management System (EDMS)
  • Adobe Acrobat
  • Communication
  • Customer Service
  • Detail-Oriented
  • Adaptability
  • Improvement Projects
  • Process Improvements
  • International Standardization
  • Management Process
  • Audits Compliance
  • Employee Training Programs
  • Global Communications
  • Maintenance Management
  • Pharmacovigilance
  • Project Management

Nice to have

  • Ennov Insight Publisher
  • Lorenz Docubridge
  • other publishing tools
  • regulatory registration procedures in the EU and EEMEA regions

What the JD emphasized

  • publishing experience
  • tight deadlines
  • critical submission targets