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we are looking for an Algorithms Engineer to join our team.

In this role you will:

Be part of a leading Algorithm team responsible for developing Radio core technologies for innovative wireless communication products.

Develop algorithms and architectures for a high spectral efficiency modem in a challenging environment.

Simulate & test new HW & SW designs in Matlab & real-time in a full modem and channel environment.

Work with the VLSI, RF, SW & System groups.

End to end involvement from the concept stages to the fully operational system.

We are looking for talented verification engineer which have abilities to own complex tasks on one hand and on the other hand be a team player, working with different vertical team and disciplines.

In this role you will be:

Responsible for the Verification of Various IPs and top level designs.
Defining and implementing the Environment architecture.
Defining and implementing Test plans, coverage plans, etc

we are seeking for a creative, curious and innovative experienced Algorithms Intern to join our Algo department.

In this role you will

Be part of a leading Algorithm team responsible for developing Radio core technologies for innovative wireless communication products.
Develop algorithms and architectures for a high spectral efficiency modem in a challenging environment.
Plan & create code generation scripts, verification tools, automations and every other tool needed by the algorithm team.
Develop and Implement software based algorithms on the MODEMs DSPs and CPUs
Work with various multidisciplinary Ceragon teams (VLSI, RF, SW & System)

looking for an Obesity Medical Scientific Liaison for the center-south region. In this role, you will be responsible for delivering high level medical and scientific expertise to internal and external stakeholders, within the obesity therapeutic area. You will be responsible for internal insight generation, scientific communications, and regional medical activities. In addition, you will work most of the time in the central and southern region of Israel with an 80 percent work rate in the field.
Your main accountabilities will be:
Development of professional relationships with external key opinion leaders and other stakeholders.
Leading scientific dialogue with key opinion leaders, including scientific presentations and personal meetings.
Identification of healthcare professional influencers within the obesity therapeutic area.
Drive internal and external scientific updates.
Drive local, regional, and international medical meetings and activities.
Generate insights from the field and participate in internal medical strategic planning.

As a Start-Up Team Manager, you will be responsible for executing the Start-Up team activities in clinical trials performed in Israel, ensuring compliance with local regulations, ICH-GCP, procedures and protocol requirements.
In addition, you will have the following responsibilities:
Manage and lead the Start-Up team, set and monitor performance targets and KPIs for the team and functional area in close cooperation with Israels Clinical Development Center (CDC) Director and with the Therapeutic Area (TA) Heads.
Ensure preparation and submission of local Clinical Trial Application to Health Authorities and Ethics Committees (ECs) to obtain all necessary regulatory approvals within defined timelines.
Deliver reliable, high-quality data and ensure study participants protection to activate sites prior to FPFV (First Patient First Visit) in the country.
Manage the lifecycle of clinical trial agreements/contracts, including sub-contractors, across trials.
Execute regulatory submissions of Clinical Trial Applications (CTA) and ongoing submissions and obtaining approvals.

As the Israel CDC Therapeutic Area Head, you will manage and lead the clinical research Therapeutic Area team and ensure that all clinical trial activities are carried out in compliance with all policies, procedures and local requirements.
You will also have the following responsibilities:
Ensure Clinical Therapeutic Area team set-up as per procedures and local regulatory requirements, unit processes & systems, resources and conduct of clinical trials in the CDC.
Drive implementation and execution of CDC trial delivery strategies and make sure risk plans are in place when needed in close cooperation with the CDC director.
Ensure performance management of the Clinical Therapeutic Area team, while guaranteeing the Clinical Research Unit goals are met.
Develop and maintain partnerships and effectively communicate with internal stakeholders, as well as external such as investigators, vendors, clients, KOLs, Ethics Committees and Health Authorities.
Inform internal stakeholders about trial/project related issues and the local therapeutic business scenario covering any current and/or potential changes in local trial related regulation.