As Medical Affairs Manager (MAM), you are a key member of the Israeli Medical team and represent an office but also field and customer-focused role, enabling medically oriented interaction with internal and external stakeholders based on individual contacts, educational events, and medical projects.
You will provide expert medical support, including educating the local sales and marketing team as needed. You will be an expert on the disease areas under their responsibility and will ensure their knowledge is current and thorough.
You will lead a medical customer engagement strategy and the medical affairs project plan for medical launch excellence and successful life cycle management that is fully in line with brand strategies and company objectives to meet the predefined targets of the affiliate medical affairs department.
Responsibilities
Medical knowledge and expertise regarding the therapeutic area and the product for which you are responsible, 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
Working in close collaboration and being part of a cross-functional team with the Marketing and Market Access Departments
Participating in national and international partners' meetings
Acting as a focal point for medical know-how by regularly reviewing clinical articles and attending scientific and medical meetings and conferences
Providing medical and scientific training and/or support to other team members across all company functions
Evaluating scientific materials, preparing for lectures and presentations
Providing medical information and, if necessary, forwarding medical questions to partners abroad
Maintaining scientific and medical contact with key opinion leaders and decision-makers
Writing an annual medical plan together with the Medical Lead/ Medical Director and in coordination with the marketing department
Proactively supporting business development team and processes
Working in collaboration with the regulatory department
Participating in the process for inclusion of technologies in the health basket
Leading Early Access Programs, compassionate use programs and clinical trials
Reporting any safety information received to the Pharmacovigilance Department
Working in accordance with all compliance rules with local and global partners' regulatory guidelines
Requirements: MD / PhD in life science / DMD / PharmD / VMD
Relevant experience in the biotech/pharma industry
High level of English and Hebrew
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
Team player
This position is open to all candidates.