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Medical Information & Pharmacovigilance Specialist Germany BiomapasJoin our global team as a Medical Information and Pharmacovigilance Specialist for Germany market.. 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 or Denmark), 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) . ·     Preferably at least 1-2 years experience in medical information and/or pharmacovigilance. ·     Fluent written and spoken English and German language. ·     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 Company Location: Germany.