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Medical Information Specialist - Danish speaker

biomapas·Romania

remoteEMEA hours

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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
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