Medical Affairs Manager

At Medison, we are team players, working together across countries, cultures, and time-zones to carry out our mission to help patients who suffer from the most challenging diseases. We welcome you to join us!

About This Role

As Medical Affairs Manager – Neuroscience, you will act as the medical interface, providing scientific and clinical management of products in the Neuroscience unit. You will be a crucial function that works within a cross-functional environment, effectively linking science and commercial activity. Your role is to harness the scientific and clinical expertise, to build strong professional relationships with external and internal stakeholders. This enables information and data to be communicated in high standards and according to strict compliance principles between the company and the medical stakeholders and for valuable input to be gathered. You will work closely with marketing team and other functions in the company. You will manage the medical relationship with the medical counterparts of the partners abroad and support the marketing teams in their interaction with the partners.

What You Will Do

• Provide medical knowledge and expertise regarding the therapeutic area and the product for which you are responsible for, including elements such as staying updated on the medical developments in the field, clinical and research information and sharing the knowledge with the relevant team members
• Work in close collaboration and be part of a cross functional team with the Marketing and Market Access Departments
• Participate in national and international partners’ meetings
• Focal point for medical know-how by regularly reviewing clinical articles and attending scientific/medical meetings and conferences
• Provide medical and scientific training and/or support to other team members across all company functions.
  • Evaluate scientific materials, preparing for lectures / presentations
  • Provide medical information and, if necessary, forward medical questions to partners abroad
• Maintain scientific and medical contact with key opinion leaders and decision makers
• Write an annual medical plan together with the medical lead/ medical director and in coordination with the marketing department
• Proactively support business development team and processes
• Work in collaboration with the regulatory department
• Participate in the process for inclusion of technologies in the health basket
• Lead Early Access Programs, compassionate use programs and clinical trials
• Report any safety information received to the Pharmacovigilance Department
• Work in accordance with all compliance rules with local and global partners’ regulatory guidelines

Qualifications

Required Skills

• MD / PhD in life science / DMD / PharmD / VMD
• High level of English – Mandatory
• Excellent organizational, planning, and project execution skills, with an aptitude for details, and an ability to multitask and prioritize in a fast-paced environment
• Excellent interpersonal and presentation skills
• Dynamic and team player

Preferred Skills

• Relevant experience in the Biotech/ Pharma industry  – Advantage