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At Medison, we offer hope to patients suffering from rare and severe diseases. Through strategic partnerships with best-in-class biotech companies we commercialize innovative therapies across global markets. Medison is a dynamic, fast?paced company operating in dozens of countries across five continents. We are looking for passionate, agile, and adaptive leader who want to make a real impact and help shape the future of global healthcare. Our culture is rooted in care, agility, collaboration, and innovation, and we’re united by a shared purpose to make a meaningful difference. If you’re passionate about driving growth and delivering breakthrough innovation to patients, we invite you to be part of our journey. Reporting to Medison’s Head of Business Development, the Director, Search & Evaluation Business Development is a mission?critical leadership role that directly shapes Medison’s long?term growth and strategic direction, while advancing our core purpose of improving and saving patients’ lives worldwide. The position plays a foundational role in building Medison’s future pipeline by identifying high?impact opportunities that expand global access to the most advanced therapies. In this role, you will proactively identify best?in?class assets, lead rigorous scientific and clinical evaluations, and drive cross?functional diligence to enable high?quality, strategic partnering decisions. You will operate at the intersection of science, strategy, and execution, working in close partnership with Medical, Regulatory, and senior leadership to support disciplined growth and long?term value creation.

Responsibilities:

* Proactively screen, source, and prioritize best?in?class late?stage assets from Phase 2 through marketed products across rare and severe diseases, leveraging multiple platforms, databases, and industry sources.
* Build and manage a robust and high?quality pipeline of partnership opportunities aligned with Medison’s long?term growth strategy.
* Lead rigorous scientific and clinical evaluations by assessing clinical data versus current standard of care, mechanism of action differentiation, regulatory pathways, and competitive landscape.
* Develop clear and data?driven Target Product Profiles (TPPs) to support scientific, clinical, and strategic positioning.
* Conduct comprehensive research, including literature review and data synthesis, to deeply understand disease biology, unmet need, and therapeutic value.
* Engage directly with Key Opinion Leaders, clinical investigators, and external experts to validate assumptions and strengthen scientific and clinical assessments.
* Drive cross?functional diligence by partnering closely with function leads, Medical and Regulatory, Commercial, Legal, Finance, and other relevant stakeholders.
* Support transaction strategy and execution by providing scientific and clinical input into transaction strategies, diligence materials, and contractual discussions.
* Prepare clear, concise, and decision?ready materials, including evaluation summaries, one?pagers, presentations, and business cases for senior leadership and governance forums.
* Continuously refine and strengthen Search and Evaluation processes, criteria, and scientific convergence frameworks to improve rigor, consistency, and speed of decision?making.
* Act as a trusted thought partner to leadership by surfacing insights, risks, and recommendations that directly influence portfolio strategy and Medison’s growth trajectory.
* Represent Medison externally in partnering discussions, scientific meetings, and industry conferences to strengthen Medison’s visibility and network.

City:
Petah Tikva

Exciting opportunity to be part of Imaging Informatics regulatory team. Imaging Informatics
business unit includes solutions for radiology and cardiology. From enterprise imaging, PACS, and
workflow orchestration, through to a full suite of solutions for the cardiovascular workflow, we deliver
optimized imaging service lines that enable enterprise imaging across sites, specialties and technologies
to simplify medical image management, enable effective collaboration and enhance patient care. This role
will focus on radiology regulatory activities.


Responsibilities:
Represent regulatory affairs at the Radiology Informatics leadership team
Through end-to-end regulatory processes, ensuring safe and effective products are brought to
market, on time, and sustained throughout life cycle via compliant, innovative regulatory
strategies
Manage day-to-day functioning of radiology regulatory team ensuring effective and efficient
execution
Provide critical input on regulatory risk assessments to support portfolio selection and post
market decision making
Build proactive, strategic relationships with external stakeholders (Notified Bodies, FDA,
Competent Authorities, etc.) to ensure that requirements are known early during strategy
development, which enables fast market access with the current portfolio in connection with
future innovations.
Lead and enable strong cross-functional partnership between regulatory affairs and all key
stakeholders including R&D, Product Management, Quality, Clinical Affairs, and other functions at
all levels within the business, and the local Regulatory Affairs teams in the market
organization.
Mentor and develop regulatory talent and competency to ensure strategic engagement and
execution excellence