Medical Information Specialist - Danish speaker
This is the employer's own posting, not a copy on a job board.
What we know
Is it still open?
Confirmed still open
Last checked 21h ago — checked against the employer's own applicant tracking system, which is the company answering directly.
We re-read the employer's own applicant tracking system and the posting was still there. That is the company answering directly.
How old is it?
Posted 24d ago
The date the source published, not the day we noticed it (2026-09-17). Last seen at its source just now.
We have tracked this listing since 17 Sep 2026 (23 days). The employer's own board has carried it every time we have read it, most recently just now.
Is it remote?
Marked remote on the employer's board
Their board carries a remote setting on this posting — a field they filled in, not wording we read. The location field names somewhere specific, which is usually where the team or the entity sits.
Who may apply?
Sweden, Norway, Denmark, Germany, Poland, Romania
The description states no restriction of its own. This is the source's own tag.
Carried by 1 source
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Workable employer's own board first seen 23d ago · last seen just now
The listing
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
Requirements
- 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
Benefits
- 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