Specialty
The role
TransPerfect is hiring a senior medical writer to lead clinical regulatory documents for pharma and biotech client teams. This is a remote role for applicants in Brazil.
What you will do
- Plan and lead preparation of clinical regulatory documents
- Coordinate client contributors and internal QC and publishing
- Run kickoff and comment resolution meetings
- Conduct literature searches and peer QC reviews
What they ask for
- 5+ years as a medical writer in CRO, biotech or pharma
- Bachelor's degree or higher in a relevant field
- Experience writing CSRs, protocols, investigator brochures and module 2/5 documents
- Knowledge of ICH and US regulatory requirements
- Experience with document management and collaborative authoring tools
- Strong written and spoken English
This is our own short reading of the posting. The full description, and anything that has changed since, is on TransPerfect's careers page behind the apply button.
