Medical Information and Pharmacovigilance Specialist

The Medical Information (MI) and Pharmacovigilance (PV) Specialist acts as a 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 ensuring compliance, exchanging safety information, and serving as a contact for timely safety processing.

The position is remote for the Nordic countries (Sweden, Norway, Denmark, or any EU country), working in close collaboration with Finland and Iceland’s local medical information and pharmacovigilance support personnel.

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 and external partners
• Ensure compliant execution of all MI and PV operational activities at a 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

Requirements

• A degree (preferably a master’s) in a 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 and 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 work
• Complimentary health and wellness benefits, such as influenza vaccines
• Rewarding referral policy
• Workplace establishment allowance (fully remote)
• Team building, global meetings, and B active events