Medical Information and Pharmacovigilance Specialist (Nordics)

Join our global team as a Medical Information and Pharmacovigilance Specialist in Nordics.

Medical Information (MI) and Pharmacovigilance (PV) 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 and PV 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
• Review local literature and act as a local safety officer serving as the main contact for safety matters with authorities and customers, as applicable

• 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