GSK | Reino Unido
| Salud, Inglés
“GSK seeks an experienced Principal Medical Writer to author and deliver high-quality clinical regulatory documents (protocols, CSRs, Investigator's Brochures) and lead CTD submission dossiers. Requires PhD or equivalent in life sciences, advanced regulatory medical writing experience, and strong understanding of clinical trial design, ICH guidelines, and statistical analysis. Offers hybrid work model, competitive salary (CAD 118K-168K), bonuses, healthcare, pension, and shares/savings program.”