Senior Medical Affairs Manager, Onco-Hemato, Israel at Medison Pharma

Petah Tikva, Center District, Israel -

Full Time

Start Date

Immediate

Expiry Date

22 Jul, 26

Salary

0.0

Posted On

23 Apr, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Medical affairs, Clinical expertise, Scientific communication, Relationship management, Key opinion leader management, Project execution, Strategic planning, Marketing collaboration, Regulatory compliance, Clinical trials, Medical information, Presentation skills, Problem-solving, Multitasking, Teamwork, Data analysis

Industry

Pharmaceutical Manufacturing

Description

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! The Medical Affairs Manager is the medical face of the company. His/her value lies in his/her scientific and clinical expertise and ability to build strong relationships with the community and academic physicians. This allows for information to flow freely between the medical community and the company. The Medical Affairs Manager works closely with the marketing team. He/She manages the medical relationship with the medical divisions of the partners abroad. Responsibilities Medical expertise regarding the assigned therapeutic area and product, including keeping updated on medical developments in the field, clinical and research information, and sharing it with the marketing teams. Participation in national and international medical conferences. Participate in formalizing medical and marketing strategy through analysis of scientific materials. Instructing physicians before relevant presentations. Meetings with Medison’s business partners in Israel and abroad. Provide training to the marketing teams on topics relevant to the marketed products Maintaining scientific and medical contact with key opinion leaders (KOLs) and decision makers. Serve as the local medical information service for the assigned products, and answer medical questions according to the policy signed with the relevant business partner. Create and execute an annual medical plan for each product. Supporting business development processes. Supporting the inclusion of products into the national health basket in coordination with the regulatory and market access departments. Working in collaboration with the Marketing and Market Access Department Working in accordance with all compliance guidelines, including local and partner regulatory guidelines Leading early access programs and clinical trials feasibility. Requirements Required education and experience Doctor of Medicine (MD) / PhD in life science / Doctor of veterinary medicine (DVM) / Doctor of dentistry medicine (DMD) / Pharm.D Relevant experience in the pharma industry is required- at least 2 years Required skills 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 Team player Problem-solving and a constant improvement mindset Work independency High level of English proficiency- oral and written

Responsibilities

The Medical Affairs Manager serves as the primary scientific face of the company, building relationships with medical professionals and key opinion leaders. They are responsible for developing medical plans, supporting marketing strategies, and ensuring compliance while managing clinical trial feasibility and medical information.