Senior Director / Executive Director Medical Writing

📋 Description

• Lead the PV Medical Writing function, ensuring high-quality, compliant, and timely deliverables.
• Manage and develop the PV Medical Writing team, fostering performance, engagement, and professional
• Drive quality, compliance, inspection readiness, and continuous improvement initiatives, including
• Provide strategic PV medical writing expertise and subject matter leadership to clients, internal
• Support business development activities, including proposals, bid defenses, and client engagements.
• Oversee departmental resources, budgets, and operational performance to ensure efficient service

🎯 Requirements

• Master’s degree in life sciences or healthcare, PhD preferable.
• Extensive pharmacovigilance and PV Medical Writing experience, including leadership and people
• Deep knowledge of global pharmacovigilance regulations, with expertise in authoring and reviewing
• Proven experience supporting regulatory compliance, inspections, and pharmacovigilance system
• Strong business acumen with experience supporting proposals, client engagements, and bid defense
• Excellent scientific, regulatory, and analytical capabilities, including translating complex

🎁 Benefits

• Global pharmacovigilance specialist with presence across Europe, North America, South America, Asia
• Culture built on kindness, flexibility, growth and belonging; supportive colleagues; ideas heard
• Value-driven environment emphasizing Quality, Integrity, Drive, Agility, Belonging, and
• Opportunity to contribute to patient safety from early development through post-marketing