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Senior Medical Writer

Kuala Lumpur Job No. 14257234 Full-time - On-Site

工作描述

Join us in shaping impactful, evidence-based content that drives meaningful engagement. As a Medical Writer, you will contribute to the development of high-quality, compliant medical content within the healthcare and pharmaceutical landscape. Working alongside cross-functional teams, you will support the delivery of accurate, audience-appropriate materials while continuing to build your expertise in clinical and regulatory writing.

Key Responsibilities:

  • Develop high-quality, evidence-based content for healthcare professionals (HCPs) and healthcare consumers (HCCs) across multiple platforms, ensuring clarity, scientific accuracy, and regulatory compliance.
  • Support alignment with Medical, Legal, and Regulatory (MLR) requirements by incorporating appropriate claims, references, and disclaimers into content.
  • Conduct literature searches and support the identification and summarization of relevant scientific references to inform content development.
  • Collaborate with cross-functional teams (Content Strategists, Visual Designers, Copywriters, Medical Affairs, and Project Managers) to ensure content aligns with strategic and communication objectives.
  • Review and edit materials for accuracy, consistency, and alignment with brand and regulatory standards prior to submission for approval.
  • Incorporate feedback from senior team members and stakeholders to refine content and ensure quality standards are met.
  • Contribute to internal knowledge sharing and support junior writers where appropriate.
     

职位要求

Job Requirements:

  • Minimum 4–5 years of experience in clinical and/or medical writing within the pharmaceutical or healthcare industry.

  • Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Medicine, Public Health, or a related field.

  • Solid foundation in clinical and/or regulatory medical writing.

  • Experience developing scientific or pharmaceutical content for HCPs and/or HCCs.

  • Working knowledge of medical regulatory requirements and MLR processes.

  • Strong attention to detail, scientific accuracy, and ability to interpret and communicate complex data clearly.

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