Senior Director / Executive Director Medical Writing

📋 Description

• Lead the PV Medical Writing function ensuring high-quality, compliant, timely deliverables.
• Manage and develop the PV Medical Writing team for performance and growth.
• Drive quality, compliance, inspection readiness, and continuous improvement incl. SOPs, KPIs
• Provide strategic PV medical writing expertise to clients, stakeholders, and project teams.
• Support business development via proposals, bid defenses, and client engagements.
• Oversee resources, budgets, and operational performance for efficient service delivery.

🎯 Requirements

• Master’s degree in life sciences or healthcare; PhD preferred.
• Extensive pharmacovigilance and PV Medical Writing leadership experience.
• Deep knowledge of global pharmacovigilance regulations; expertise in aggregate safety reports and
• Experience with regulatory compliance, inspections, and PV system oversight; QPPV or Deputy QPPV
• Strong business acumen with proposals, client engagements, and bid defense experience.
• Excellent scientific, regulatory, and analytical abilities; ability to translate data into clear

🎁 Benefits

• Global pharmacovigilance environment with patient safety at the center.
• Collaborative, growth-oriented culture across multiple regions.
• Opportunity to engage with clients, industry peers, and professional development.