Become a key player at Alsinova as a Clinical Medical Writer in Belgium, collaborating on various healthcare research documents for leading clients. Showcase your writing talents and scientific knowledge.
You’ll be responsible for synthesizing information into reports, drafting clinical trial documents, and providing quality control. Your role will involve working closely with both clients and authors while ensuring compliance with established standards of good clinical practice. Bring your knowledge of oncology and your ability to communicate complex data in French and English.
Key Responsibilities:
• Draft and review clinical development documents
• Synthesize literature into actionable reports
• Lead the review process of clinical documents
• Update templates and processes as required
• Facilitate client communications regarding scientific content
Requirements:
• At least one year of medical writing experience essential
• Scientific degree critical for ...