About this role
Clinical Trial scientific writer at MEDSIR. Location: Barcelona, Catalonia, Spain. Role: developing protocols, reviewing documents, registering trials Requirements: MSc in health sciences required (PhD preferred); strong clinical research knowledge, protocol and medical writing skills, familiarity with ICH/GxP, MS Office and literature searching, and strong communication skills in English. Category: Research and Development (R&D) Seniority: Senior Level Tools: Microsoft Office, ClinicalTrials.gov, GoodHabitz, Cobee, Wellhub, MacBook Commitment: Full Time Workplace: Hybrid Languages: English