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Senior Medical Writer

Content Development Senior Analyst | Early Career | Full time
ジョブ番号 14257234 | Kuala Lumpur
応募する

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.

Kuala Lumpur

雇用機会の均等化に関する声明

アクセンチュアは選考に際し、適用される法令に基づき、応募者を年齢、人種、思想信条、肌の色、宗教、性別、国籍、出生地、民族的起源、障がいの有無、性的指向、性同一性、遺伝情報、婚姻、パートナーの有無、市民権において差別することなく、全ての応募者に対し適用される法令に基づき採用選考を行います。

We work with one shared purpose: to deliver on the promise of technology and human ingenuity. Every day, more than 775,000 of us help our stakeholders continuously reinvent. Together, we drive positive change and deliver value to our clients, partners, shareholders, communities, and each other.

We believe that delivering value requires innovation, and innovation thrives in an inclusive and diverse environment. We actively foster a workplace free from bias, where everyone feels a sense of belonging and is respected and empowered to do their best work.

At Accenture, we see well-being holistically, supporting our people’s physical, mental, and financial health. We also provide opportunities to keep skills relevant through certifications, learning, and diverse work experiences. We’re proud to be consistently recognized as one of the World’s Best Workplaces™.

Join Accenture to work at the heart of change. Visit us at www.accenture.com.

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