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We're looking for a talented Senior C++ Developer with a deep foundation in research engineering and Linux kernel.
As a Senior C++ Developer you will be responsible for:
Designing, implementing, and optimizing our eBPF Agent.
Conducting research focused on Linux kernel internals, eBPF, and related technologies.
Writing clean, efficient, and maintainable C++ code, with a focus on low-level and systems programming.
Collaborating with data scientists, system architects, and product managers to translate technical requirements into robust, scalable solutions.
Using a profiling and debugging tools to analyze and optimize the performance of our agent.
Documenting code and research insights to support knowledge sharing across the team and facilitate continuous development.

Required Senior Site Reliability Engineer
Israel (Remote)
Job Description
Are you excited by the prospect of working with innovative security products?
Do you enjoy creating innovative and strategic solutions to solve complex problems?
Join Our Site Reliability Engineers Team
We are redefining how organizations protect data centers and clouds from advanced threatsdriven by our exceptional people. Join our Cloud team to build a high-performance SaaS platform that enables faster releases, large-scale deployments, and effective monitoring.
Partner with the best
Our Cloud team is a diverse team that includes both SREs and Software Engineers. As part of our ongoing innovation efforts, we are also developing cutting-edge AI agents that enhance R&D productivity, automate complex workflows, and improve operational efficiency across the organization.
As a Senior Site Reliability Engineer, you will be responsible for:
Developing, improving, and maintaining Guardicore's Cyber Security SaaS platform. Troubleshooting multiple Kubernetes platforms.
Practicing infrastructure as a code (IaC) using Terraform and GitOps, utilizing ArgoCD to automate and manage infrastructure.
Evolving our tooling, logging, monitoring, and alerting systems to increase observability and transparency.
Coding internal tooling using multiple programming languages (GoLang/Python/etc).Triaging and Solving platform issues during day-to-day operations.
Collaborating with Guardicore's Development and Research groups to constantly improve our platform.
Contributing to the development and integration of advanced AI agents that streamline R&D processes and increase engineering efficiency

Required Principal Security Researcher - Enterprise Security Research
Israel (Remote)
Job Description
Are you excited to lead impactful security research and share your discoveries at leading global conferences?
Are you passionate about uncovering attack surfaces, breaking complex software, and presenting your findings at conferences such as Black Hat, DEF CON, and RSAC?
Join the Enterprise Security Group
Our Enterprise Security Group focuses on protecting enterprise environments at scale, combining deep network visibility, micro-segmentation, and threat intel. Our research is driven by large-scale, real-world data from top enterprises across the globe.
Join our Security Research Team:
As a member of our research team, you will investigate emerging attack surfaces across operating systems and modern technologies.
You will reverse engineer complex software, discover vulnerabilities, and develop original research.
Researchers are encouraged to explore new ideas and transform promising findings into published research shared with the global security community.
In this role you will be:
Leading end-to-end research projects - from idea generation, through discovery and exploitation, to publication
Conducting deep security research across operating systems, cloud environments, enterprise software, and emerging technologies
Developing proof-of-concepts and research tools
Leveraging AI to scale research workflow
Publishing research via technical blogs, whitepapers, and top-tier conferences
Collaborating with detection and product teams to translate research into security capabilities

Required Senior Data Scientist- Flex
Israel (Remote)
Job Description
Do you enjoy working with huge datasets to develop models and agents to solve complex problems?
Are you excited to work with innovative web security products?
Join our team!
The App&API Security team is responsible for the continuous research and development of the Web Application Firewall. We serve thousands of large enterprise customers.
In this role you will:
leading the development of data science aspects in the product, working as part of the multidisciplinary research team. You will be responsible for the development and maintenance of models and agents. Adding innovation and advanced models, and developing DS tools to provide insights and analysis of web security attacks.
Responsibilities:
Leading and collaborating on end-to-end projects across the team and with engineering and product partners, from initial concept through to final deployment
Developing working prototypes of statistical/machine learning-based algorithms, evaluating and comparing metrics based on real-world data sets
Developing agentic systems to enhance detections and research paths
Guiding engineering implementations of autonomous security agents
Working closely with security researchers to combine subject matter expertise into the models
Working to integrate security research learnings into the product
Innovating in the web security research and data science space
Providing DS expertise to the wider web security research group.

We are seeking a high-calibre Senior Counsel, Employment to join our scaling Legal Department. The role is remote and the role-holder will be based in either UK, France, Spain, Israel or Ireland. In this strategic role, you will counsel CrowdStrikes business leaders and the HR team on employment matters across 21 EMEA jurisdictions. The role involves all aspects of the employer-employee relationship You will help resolve disputes and have the opportunity to manage outside counsel around the world. You will collaborate with stakeholders to lead cross-functional initiatives and manage interesting and complex projects from inception to implementation. The position will report to the Assistant General Counsel EMEA (Employment).


What Youll Do:

Act as one of our three employment lawyers in the EMEA region and provide additional support for other regions as necessary.

Be a strategic adviser and contact to business leadership and the HR team on a wide-range of employee relations matters providing commercially-driven legal solutions that balance risk with rapid business growth.

Draft and review employment agreements, separation agreements, and corporate policies.

Advise on recruitment, terminations and performance management cases, internal investigations and disciplinary issues, and global labor law compliance.

Run the employment aspects of M&A deals.

Lead and oversee complex multi-jurisdictional projects.

Manage litigation for employment law disputes.

Support the HR, Sales, Finance, Payroll, Benefits, and Equity teams with various projects.

Work with the Compensation team to draft, review, and revise variable compensation plans.

Collaborate with the Human Resources team to conduct training.

Stay up-to-date on developments to laws throughout the region.

We have a vacancies for (Senior) Project Managers in our Neuroscience Team in the EMEA region.

Ideally we seek indication experience in the following areas for these roles (please note in your application your experience in any of the following):

Rare Disease: Myasthenia Gravis, Huntington's, ALS, DMD, CIDP, DM1 (myotonic dystrophy) and FSHD - CAR-T experience

Ophthalmology: General ophthalmology, Diabetic Macular Edema & Geographic Atrophy

Sleep, Epilepsy and psychiatry

Basket, Master Protocol or Adaptive Trial experience is an advantage


Discover Impactful Work:
Serves as the Project Lead and primary sponsor contact. Accountable for the overall delivery of the project (quality, time, cost) on behalf of the organization. Establishes and communicates customer expectations to the project team. Leads the cross functional project team to meet or exceed deliverables.

A day in the Life:

Is the primary contact between the sponsor and the organization at the project level.

Ensures escalation pathways adhered to internally and externally (Rules of Engagement - communication pathways).

On projects where the scope requires, ensures clear delineation in responsibilities and communication pathways for secondary project leads (such as lead in a specific region, lead for a specific vendor(s) or subset of delivery).

Ensures financial stewardship at a project level by demonstrating an intimate understanding of the contract, resource alignment to budget, management of Out of Scope activity, drive the Con Mod process/negotiations and team execution to timelines.

Establishes, communicates and manages the sponsor to achieve optimal delivery during the project

Drives Risk Identification and Issue Resolution at project level (RBQM/RESOLVE).

Ensures project team compliance with organization policies, SOPs, ICH- GCP, regulatory and project specific requirements.

As a Country Approval Specialist, you will participate in the management and preparation, review and coordination of Country Submissions in line with global submission strategy in order to activate investigative sites. You have a strong attention to detail, taking ownership of the accuracy of these documents while holding yourself and others accountable.

Supporting the facilitation of site start up and communication with internal and external team mem-

bers to ensure prompt site approval and study timelines are achieved.

Support sites and study teams to achieve rapid site start up

Essential Functions:
Prepares, reviews and coordinates, under guidance, local regulatory submissions (MoH, EC, additional special national local applications if applicable, e.g. gene therapy approvals, viral safety dossiers, import license) in alignment with global submission strategy.
Provides, under guidance local regulatory strategy advice (MoH &/or EC) to internal clients.
Provides project specific local SIA services and coordination of these projects.
May have contact with investigators for submission related activities.
Key-contact at country level for either Ethical or Regulatory submission-related activities.
Coordinates, under guidance, with internal functional departments to ensure various site start-up activities are aligned with submissions activities and mutually agreed upon timelines; ensures alignment of submission process for sites and study are aligned to the critical path for site activation.
Achieves PPDs target cycle times for site.
May work with the start-up CRA(s) to prepare the regulatory compliance review packages, as applicable.
May develop country specific Patient Information Sheet/Informed Consent form documents.
May assist with grant budgets(s) and payment schedules negotiations with sites.
Supports the coordination of feasibility activities, as required, in accordance with agreed timelines.
Enters and maintains trial status information relating to SIA activities onto PPD tracking databases in an accurate and timely manner.
Ensures the local country study files and filing processes are prepared, set up and maintained as per PPD WPDs or applicable client SOPs.
Maintains knowledge of and understand PPD SOPs, Client SOPs/directives, and current regulatory guidelines as applicable to services provided.

Leads the local study team consisting of within-country clinical operations team members, cross-functional experts (medical, regulatory, supply logistics, finance, legal, etc.), vendor staff, and external clinical site staff involved in study preparation and delivery providing both matrix leadership and project management of study activities within the country(ies).
Serves as the operational point-of-contact between the central study team and within-country(ies) study team. The LDL collaborates closely with local medical and regulatory affairs staff to align local medical and scientific requirements. As required, collaborates with the local and above-country teams for conducting study feasibility and site selection within country(ies). Leads selection of sites within country(ies) and is accountable for local study performance.
Accountable for within-country delivery of assigned studies to time, budget, and quality expectations as defined in the clinical development plan and study protocol as well as in local/regional regulations, IND/GCP/ICH-guidelines, and procedures. Ensures quality and integrity of clinical studies by taking on appropriate business management monitoring activities.
Ensures development and maintenance of country study plan and that critical study timelines related to study activities within-country(ies) are accurately forecasted and achieved, including budgets, resource estimates, milestones, timelines, quality and risk planning, and that recruitment targets, patient recruitment cycle times, data, and audit/inspection quality are met. Provides troubleshooting and problem resolution support for within-country study team to ensure productive, efficient study delivery. Ensures necessary supplies are available at sites and manages local supply inventory.
Accountable for the accuracy of study systems, including completeness of the trial master file, and reporting study delivery progress to study team and key stakeholders and to specify and review in-country study monitoring tracking tools, monitors key risk and performance indicators, and other reports. Review all study databases to ensure 100% accuracy.
Ensures development of country/site-level risk assessment to proactively identify risks, develop a mitigation plan, and escalate issues and risks that may impact study delivery.
Will review and approve monitoring visit reports and ensure appropriate site monitoring activities have been completed per the study monitoring plan.
May provide feedback on performance, capabilities, and competencies of local study members to line management.