Medical Information Specialist - Danish speaker

Biomapas · Sweden · posted Sep 17, 2026

Open to candidates in 28 countries

Austria, Belgium, Bulgaria, Croatia, Cyprus, Czechia, Denmark, Estonia, Finland, France, Germany, Greece, Hungary, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway, Poland, Portugal, Romania, Slovakia, Slovenia, Spain, Sweden

Full-timejunior

You apply on the company's own site. We never charge to apply.

What this role actually asks for

Extracted by RemoteHunt

Must have

  • •Fluent written and spoken English and Danish
  • •1-2 years experience in medical information/pharmacovigilance
  • •Degree in Life Science field
  • •Attention to detail & time management
  • •Excellent knowledge of local and international regulations

Nice to have

  • •Swedish and Norwegian languages proficiency beneficial
  • •Analytical skills

Languages required

enda

The full posting

Join our global team as a Medical Information Specialist for Nordics. Medical Information (MI) Specialist acts as product specialist interfacing with external stakeholders (HCPs and patients) to develop and provide concise, accurate, and non-promotional medical information responses in a timely manner, while also ensuring compliance, exchanging safety information and serving as a contact for timely safety processing.

Position is remote for the Nordic countries (Sweden, Norway, Denmark or any EU country), working in close collaboration with Finland and Iceland local medical information & pharmacovigilance support personnel. You have energy and motivation to work in a team and to gain more experience? Submit your CV in the English language for consideration.

Responsibilities

Perform key medical information contact center services Provide timely, accurate, and balanced responses to unsolicited requests for information to HCPs and patients using Biomapas or customers’ Medical Information System Analyze and interpret scientific data to update or develop comprehensive, balanced, credible and accurate response documents meeting applicable laws and procedures Exchange customer insights and scientific information with internal & external partners Ensure compliant execution of all MI operational activities at high level of quality Engage in timely handling and reporting of safety information and product quality complaints Perform local operations and ensure compliance with safety regulations and procedures Degree (preferably masters) in Life Science field (Medicine, Biomedicine, Pharmacist or Nurse) 1-2 years’ experience in medical information and/or pharmacovigilance Fluent written and spoken English and Danish languages Swedish and Norwegian languages proficiency beneficial Attention to detail & time management Effective use of appropriate IT systems and programs In-depth, demonstrated experience in most areas pertaining to good practices in medical information, pharmacovigilance and pharmacovigilance legislation Excellent knowledge of local and international regulations (ICH, EU GVP Modules) Analytical skills to understand, analyze, interpret, and present scientific data High motivation to develop and learn within the team Professional growth and career opportunities International team and environment Bonus based on annual performance Personal accident and business trip insurance Additional health insurance Remote/home based Complimentary health and wellness benefits, such as influenza vaccines Rewarding referral policy Workplace establishment allowance (fully remote) Team building, global meetings, B active events

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