Medical Information Specialist - Danish speaker

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

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...

• 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