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.

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 SystemAnalyze and interpret scientific data to update or develop comprehensive, balanced, credible and accurate response documents meeting applicable laws and proceduresExchange customer insights and scientific information with internal & external partnersEnsure compliant execution of all MI and PV operational activities at high level of qualityEngage in timely handling and reporting of safety information and product quality complaintsPerform 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 pharmacovigilanceFluent written and spoken English and Danish languagesSwedish and Norwegian languages proficiency beneficial Attention to detail & time management Effective use of appropriate IT systems and programsIn-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 environmentBonus based on annual performancePersonal accident and business trip insurance Additional health insuranceRemote/home based Complimentary health and wellness benefits, such as influenza vaccinesRewarding referral policyWorkplace establishment allowance (fully remote)Team building, global meetings, B active events