
Senior Medical Writer - FSP
Parexel seeks a Senior Medical Writer to author, edit, and manage clinical and regulatory documents (e.g., protocols, clinical study reports, CTD sections, investigator brochures, informed consents). The role includes quality control, project/document management, collaboration with cross-functional teams, and adherence to SOPs and regulatory guidelines (e.g., FDA/EMA, ICH-GCP). Requires a Bachelor's in life/health sciences and fluency in English.











