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.