We are looking for a Medical Writing Assistant/Officer Junior W/M to join our team.

(1/2 days on site)

Group 10
Responsibilities

  • Coordination of documentation related to regulatory and clinical development
  • Check documents preparation such as protocols, clinical summaries, QC that tabulating listing is working, ICS, clinical documentation; Module 1 preparation may be included
  • Knowledge on CTD

 

Example of tasks :

  • Document management with quality control and eCTD ready
  • Formatting deliverables in relation to the medical writer responsible
  • Manages the publication of study report appendices or is in contact with the CRO responsible for the publication to provide it with the necessary documents and ensure the quality of the publication
  • Conversion of documents to PDF in eCTD ready format
  • Organization of internal proofreading channels for these documents and the signature channel in connection with the medical writer in charge
  • Estimated/simulated travel costs
  • Help with document formatting and presentation preparation (power point)
  • Organization of scientific and technical meetings, team (room, invitations, equipment)

 

 

 

*non-exhaustive list*

Specialty: Drug
Therapeutic area: oncology

Group 12
Profile

  • Minimum 3 years of experience excluding periods of internship and alternance
  • Extensive knowledge of the scientific and medical environment in oncology
  • Medical and scientific writing technique
  • Analytical and synthesis skills

Medical Writing Assistant/Officer Junior W/M