
Medical Information Specialist, French & English Speaking
Posted Oct 30

Posted Oct 30
This is a fully remote position, open to applicants in United Kingdom, +6 more countries.
• Translate documents from English to the target language and vice versa.
• Provide translated responses via phone or written communication.
• Assess and address drug-information inquiries from both healthcare professionals and patients.
• Share drug information either verbally or through written correspondence.
• Identify adverse events and product complaints during customer interactions.
• Conduct intake for initial adverse-event and product-complaint reports in accordance with SOPs.
• Comply with local regulatory authority requirements for post-marketing adverse-event reporting.
• Draft narratives for adverse-event and product-complaint reports, as well as custom responses for medical inquiries.
• Manage quality-related complaint processes in collaboration with Quality Assurance, Regulatory Affairs, and complainants.
• Assess medical literature and create information tailored for healthcare professionals.
• Assist with market and competitive product research, system development, sales training, and field liaison projects.
• Engage in medical writing and fulfill assigned on-call duties.
• Enhance and maintain customer service and process metrics at the Medical Communications Call Centre.
• Degree in Life Sciences or healthcare, or an equivalent qualification.
• Solid clinical background.
• Exceptional verbal and written communication skills.
• Proficiency in English at C1 level is mandatory.
• Native or mother-tongue fluency in French is essential.
• Strong skills in translation.
• Availability to work during European hours, from 8am to 6pm CET, Monday to Friday.
• Must be legally authorized to work in the European Union or the UK.
• Willingness to travel up to 10% of the time.
• Preferred experience in call centers, Medical Information, the pharmaceutical industry, or clinical environments, including medical writing.
• Proficient in Microsoft Word, Excel, and other Windows applications.
• Previous experience with Medical Information Management Systems, Safety Databases, or similar tools is preferred.
• Capability to accurately evaluate adverse-event information requirements and the depth of data collection.
• Familiarity with safety terminology.
• Pharma D / M Pharma, BSc, or MSc in Pharmacy is preferred or considered.
• Option for home office or work at a European Hub Office.
• Day off in lieu when required to work on Bank Holidays.
• Certified as a Great Place to Work employer.
• Workplace focused on Diversity, Equity & Inclusion.
• Culture of professional development and talent enhancement.
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