DDReg Pharma

Medico-Regulatory Writer – Associate/Sr Associate

  • Providing high-quality medical and scientific writing from planning and coordination of literature search through delivery of final drafts to internal and external clients.
  • Providing technical consultation and provides substantive advice on strategy, regulations and industry best practices.
  • Demonstrate subject matter and therapeutic area expertise.
  • Effectively manage medical writing projects to deliver quality products in agreed timelines.
  • Collaborate with internal and external clients,
  • Writing CTD Modules, Medical Data Packages, SmPCs, PIs, PILs, Safety Reports, Aggregate Reports and other reports
  • Perform science review of aggregate reports produced by PV Associates
  • Ensure that document output and processes comply with client specifications, templates and styles guidelines
  • Attend project initiation meeting, collate project
  • Maintain awareness of current regulatory guidance, medical information techniques and technology relating to clinical / regulatory documentation
  • Maintain & update Aggregate Report Tracker and carry out cases reconciliation on periodic basis
  • Supporting and enabling effective and efficient communication that results in operational excellence.
  • Carry out detailed searches in regulatory agency websites like US FDA, EMA, PMDA, TGA, UKMHRA etc for safety alerts
  • Mentor Associates on job skills, oversees or develops training plans or materials for safety associates, conducts training sessions, or otherwise trains new hires and enhances the skills of existing
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