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ProPharma Group

Regulatory sciences consultant for life sciences

Mandarin Medical Information Specialist

Customer SupportUpdated on Nov 10
Full-timeRemote in AustraliaNo salary listedRemote

About the Job

Requirements

  • Native-level professional proficiency in Mandarin Chinese, including spoken communication and clear, accurate written Simplified Chinese.
  • Professional fluency in English and the ability to translate medical information accurately between English and Mandarin.
  • A qualification in pharmacy, nursing, life sciences, pharmacology, or a closely related healthcare discipline, or an equivalent relevant qualification.
  • Currently reside in Australia and be an Australian citizen, permanent resident, or holder of a qualifying long-term visa providing unrestricted full-time work rights and an ongoing right to reside in Australia without employer sponsorship or a fixed visa expiry date. Qualifying partner or spouse visas and equivalent long-term arrangements may be considered, subject to verification of visa conditions. Student visas (subclass 500), Temporary Graduate visas (subclass 485), and other fixed-duration visas do not meet the requirements.
  • Ability to work hours aligned with Mainland China business operations (China Standard Time, UTC+8).
  • Strong attention to detail, computer literacy, professional telephone communication, and the ability to follow defined quality and safety processes.

Responsibilities

  • Handle medical and safety enquiries from healthcare professionals, patients, and other stakeholders by telephone, email, and approved digital channels, delivering professional, clear, and empathetic responses.
  • Use approved product information, standard responses, relevant scientific literature, and client resources to provide accurate, balanced information in Mandarin and English.
  • Translate and proofread medical information correspondence and relevant documents between English and Mandarin Chinese, maintaining clinical meaning and quality.
  • Identify, document, and escalate adverse events, pregnancy reports, special situations, and product quality complaints under ProPharma procedures and client requirements.
  • Record enquiries and actions accurately in enquiry handling systems, meet agreed service deadlines, and perform quality checks on responses, translations, and safety-related records.
  • Follow applicable regulatory standards, ProPharma standard operating procedures, client working practices, and data privacy requirements; collaborate with colleagues on case resolution and quality improvements.

Desired Qualifications

  • Professional Cantonese proficiency, particularly for healthcare or medical communication; applicants without Cantonese are fully eligible.
  • Prior experience in Medical Information, pharmacovigilance, pharmacy, nursing, pharmaceutical customer support, or medical/scientific translation.
  • Experience supporting Mainland China healthcare or pharmaceutical stakeholders and familiarity with adverse event reporting or medical enquiry systems.

About the Company

ProPharma Group

Regulatory sciences consultant for life sciences

ProPharma Group provides regulatory sciences consulting and related services for drugs, biologics, medical devices, and diagnostics on a global scale. Its offerings cover the full lifecycle, from early development and clinical trials to regulatory approval and post-market activities. The company’s services include regulatory sciences, clinical research, quality and compliance, pharmacovigilance, medical information, and R&D technology, delivered by a team of over 2,500 professionals with more than 20 years of operation. ProPharma Group differentiates itself by providing expert, end-to-end regulatory and life sciences solutions across multiple product types and stages, helping pharmaceutical, biotechnology, and medical device companies navigate complex regulatory and compliance challenges. The goal is to help clients bring safe and compliant products to market efficiently while maintaining ongoing lifecycle support.

Company size
1,001-5,000
Company stage
Not listed
Total funding
Not listed
Headquarters
Raleigh, NC
Founded
2001

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