[Hiring] Medical Information and Pharmacovigilance Specialist @Biomapas

Role Description

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

Qualifications

• 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