לוח משרות דרושים רוקחות ופארמה בפתח תקווה

We offer hope to patients suffering from rare and severe diseases, by forming partnerships with emerging biotech companies to accelerate access to highly innovative therapies in international markets. As the creator and leader of the global partnership category in the pharma industry, we strive to be Always Ahead, and work relentlessly to bring therapy to patients in need, no matter where they live. Our values are at the core of every action we take, and we are committed to going above and beyond for the benefit of the patients we serve. We are a dynamic, fast-paced company, operating in over 25 countries on 5 continents. We are looking for out-of-the-box thinkers, people who are passionate, caring, agile and adaptive, to join us on our mission. If you are looking to make a difference in people's lives, we invite you to join us! 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 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 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, forward 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.

Medison offers hope to patients suffering from rare and severe diseases, by forming partnerships with emerging biotech companies to accelerate access to highly innovative therapies in international markets. As the creator and leader of the global partnership category in the pharma industry, we strive to be Always Ahead, and work relentlessly to bring therapy to patients in need, no matter where they live. Our values are at the core of every action we take, and we are committed to going above and beyond for the benefit of the patients we serve. We are a dynamic, fast-paced company, operating in over 25 countries on 5 continents. We are looking for out-of-the-box thinkers, people who are passionate, caring, agile and adaptive, to join us on our mission. If you are looking to make a difference in people's lives, we invite you to join us! 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 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 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, forward 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

Medison offers hope to patients suffering from rare and severe diseases, by forming partnerships with emerging biotech companies to accelerate access to highly innovative therapies in international markets. As the creator and leader of the global partnership category in the pharma industry, we strive to be Always Ahead, and work relentlessly to bring therapy to patients in need, no matter where they live. Our values are at the core of every action we take, and we are committed to going above and beyond for the benefit of the patients we serve. We are a dynamic, fast-paced company, operating in over 25 countries on 5 continents. We are looking for out-of-the-box thinkers, people who are passionate, caring, agile and adaptive, to join us on our mission. If you are looking to make a difference in people's lives, we invite you to join us! We are hiring PV Associate. Monitoring and reporting adverse events and safety information, ensuring compliance with regulatory safety guidelines and conducting activities to monitor and enhance the safety profile of Medison’s products.

Responsibilities:

* Receiving, translating, processing and documenting any reports, from overseas or locally, regarding adverse events and safety information of Medison’s products in compliance with regulatory requirements.
* Submitting timely and accurately safety reports to the Ministry of Health in compliance with local regulatory requirements.
* Actively following-up on adverse events reported by physicians and patients.
* Collecting and reviewing safety and efficacy measures taken by health authorities in recognized countries. This includes monitoring publications, regulatory updates, and safety communications from agencies such as the FDA, EMA, and other global health organizations to ensure compliance and up-to-date safety practices for pharmaceutical products.
* Reviewing relevant data from the scientific literature related to drug safety. This includes conducting literature searches to identify new safety information, adverse events, and emerging safety issues.
* Promoting awareness among healthcare professionals and medical teams regarding the importance of reporting adverse events to ensure public safety.
* Conducting periodic internal and external reconciliations
* Participating in preparations for PV audits and inspections.
* Conducting PV trainings to Medison’s employees and external suppliers.
* Additional tasks as defined by the manager