Overview
Medical Writer Jobs in Greater Kuala Lumpur at Accenture
Title: Medical Writer
Company: Accenture
Location: Greater Kuala Lumpur
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.
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.
