Senior/Lead Medical Writer

Join us in shaping impactful, evidence-based content that drives meaningful engagement. As a Senior/Lead Medical Writer, you will serve as a subject matter expert in Clinical and Regulatory Medical Writing, partnering with cross-functional teams to deliver high-quality, compliant content within the healthcare and pharmaceutical landscape. Your expertise will play a critical role in guiding key decisions, ensuring medical accuracy, and delivering innovative solutions to complex communication challenges.

Key Responsibilities

• Develop and deliver high-quality, evidence-based content for healthcare professionals (HCPs) and healthcare consumers (HCCs) across multiple platforms, ensuring clarity, scientific accuracy and regulatory compliance.

• Partner with regional and local Medical, Legal, and Regulatory (MLR) stakeholders to ensure all claims, references, disclaimers and regulatory requirements are fully met.
• Conduct comprehensive literature reviews to identify, evaluate, and annotate appropriate scientific references supporting all content.
• Collaborate with cross-functional teams (Content Strategists, Visual Designers, Copywriters, Medical Affairs, Project Managers and other stakeholders) to gather insights and ensure content aligns with strategic objectives.
• Review and edit materials to ensure accuracy, consistency, scientific rigor and alignment with brand and regulatory standards to ensure approval.
• Lead and mentor a team of writers, driving excellence in medical compliance, quality control and best practices across all developed assets.

Qualifications

• Minimum 7–9 years of experience in clinical and regulatory medical writing within the pharmaceutical or healthcare industry.
• Master’s degree in Life Sciences, Pharmacy, Medicine, Public Health or a related field.
• Advanced expertise in Clinical and Regulatory Writing.
• Demonstrated proficiency in developing pharmaceutical content for diverse audiences, including HCPs and HCCs.
• Strong understanding of medical regulatory requirements and MLR processes.