P

ProPharma Group

Regulatory sciences consultant for life sciences

Multilingual Medical Information Specialist

Medical, Clinical & VeterinaryConfirmed live in the last 24 hours
Full-timeMelbourne VIC, AustraliaNo salary listedIn-person

About the Job

Requirements

  • A degree in a life science or pharmacy, or equivalent.
  • A mother tongue in Korean.
  • Fluency in English.
  • Strong translation skills.
  • Ability to work within a team in an open and professional manner.
  • Excellent written and oral communication skills and computer literacy.
  • Sound planning, prioritising and organisational skills, including an effective workload management system and meeting deadlines.
  • Ability to take responsibility for allocated work and ensure tasks are followed through to completion.
  • Accuracy and attention to detail.
  • Ability to understand and follow processes.

Responsibilities

  • Provide a high-quality medical information enquiry handling service by answering technical questions about designated products accurately, confidently, and professionally through phone, letter, email, and fax.
  • Comply with working practices agreed with designated clients and follow processes documented in client instructions and other documentation.
  • Complete tasks within the deadlines documented in agreed ProPharma Standard Operating Procedures and Working Practices.
  • Recognise adverse events and defective product reports and handle and report them in strict compliance with agreed ProPharma Standard Operating Procedures and Working Practices.
  • Translate English documents into the target language or vice versa, and deliver translated responses by phone or in writing.
  • Use existing standard responses to prepare medical information correspondence via client databases, or liaise with the Medical Information Support Services department to request generation of correspondence.
  • Log all handled enquiries accurately, comprehensively, and promptly in enquiry handling systems.
  • Liaise with Medical Information Assistants to ensure client data is saved on file promptly where applicable.
  • Manage confidential information and personal data related to ProPharma and its clients in accordance with data privacy regulations described in ProPharma Standard Operating Procedures.
  • Maintain awareness of and comply with legal requirements and professional guidelines associated with providing medical information on behalf of the pharmaceutical industry.
  • Maintain quality in all areas of the job, particularly adverse event and product quality complaint reporting and enquiry logging.
  • Perform quality checks on adverse events, product quality complaints, and correspondence to ensure accuracy.
  • Quality-check translations in line with the translation Standard Operating Procedure.
  • Perform additional company tasks as delegated by the Manager.
  • Maintain a good working knowledge of and comply with ProPharma Standard Operating Procedures.
  • Comply with the company’s health and safety policies.
  • Adhere at all times to the employment contract’s confidentiality statement concerning data and property of ProPharma, its clients, and employees.

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

Recently Posted Jobs

Explore more opportunities at ProPharma Group

See more jobs