Principal Medical Writer

Become part of our team as a Principal Medical Writer, leading the creation of high-quality clinical and regulatory documents for complex HIV research projects. Oversee strategic planning and collaborate with cross-functional teams. Ideal for experienced professionals with a strong background in medical or regulatory writing within the pharmaceutical or healthcare sector.

Skills

• regulatory dossier development
• clinical protocols
• clinical study reports
• common technical document (ctd)
• ich guidelines
• regulatory submissions
• decision making
• clinical development
• literature reviews
• clinical trial designs
• emotional intelligence
• medical writing
• scientific writing
• influencing without authority
• communication
• strategic thinking
• pharmaceutical industry
• customer service
• learning agility
• presentation techniques
• good clinical practice (gcp)
• process improvement
• audit readiness
• kpi tracking
• statistical data interpretation
• project management
• cross-functional collaboration
• strategic planning