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We are currently seeking a Python Game Designer.
What You'll Do
Conducting in-depth mathematical creation and setting of online real money games, focusing on probability, statistics, game mechanics, features, and theory.

Calculating and optimizing online real money game probabilities, odds, and payouts, considering random number generation and statistical distributions.

Refining mathematical models that govern the mechanics and outcomes of various online real money games.

Collaborating closely with game product management, designers, developers, and stakeholders.

We're looking for a sharp and passionate Business / Product Data Analyst to join us to the product team.
Using your technical and analytical skills, you'll be responsible for telling the story behind the numbers, to understand how users interact with our products, and provide insight regarding new ideas to implement.
Responsibilities:
Be on the cutting edge of analysis, leveraging our data sources to propose new ideas that youll then see implemented.
Analyze large data sets representing users behavior, see beyond numbers and help to inform, influence, support and execute our business and product decisions.
Plan and analyze effective A/B tests in order to improve business KPIs.
Build reports and dashboards to monitor product performance, key business metrics and user experience.

We are looking for a Clinical and RA associate.
Primary function of the position:
Under the oversight of the CRA manager (CTM) the person ensures compliance of study conduct with ICH/GCP and country regulations, companys policies and procedures, quality standards and adverse event reporting requirements internally and externally.
Acts as primary site contact and site manager throughout all phases of a clinical research study, taking overall responsibility of allocated sites.
Roles and responsibilities:
Develops strong site relationships and ensures continuity of site relationships through all phases of the trial.
Performs clinical study site management/monitoring activities in compliance with ICH-GCP, Sponsor SOPs, Local Laws & Regulations, Protocol, Site Monitoring Plan and associated documents.
Gains an in-depth understanding of the study protocol and related procedures.
Coordinates & manages various tasks in collaboration with other sponsor roles to achieve Site Ready.
Performs remote and on-site monitoring & oversight activities using various tools to ensure:
Data generated at site are complete, accurate and unbiased
Subjects right, safety and well-being are protected
Conducts site visits including but not limited to initiation visits, monitoring visits, close-out visits and records clear, comprehensive and accurate visit & non-visit contact reports appropriately in a timely manner.
Collects, reviews, and monitors required regulatory documentation for study start-up, study maintenance and study close-out.
Communicates with Investigators and site staff on issues related to protocol conduct, recruitment, retention, protocol deviations, regulatory documentation, site audits/inspections and overall site performance.
Supports and/or leads audit/inspection activities as needed
Following the country strategy defined by CRD and CTM, contributes to the identification of new potential sites and works closely with them to develop strong clinical research capabilities
Whiling to travel abroad including US for sites oversights

Were looking for a brilliant and ambitious Data Scientist who is seeking his next challenge, with proven experience in big-data analysis, machine learning algorithms and digital signal processing.
We invite you to work in a creativity oriented, vibrant and non-formal environment that will encourage you to learn, grow your research and development skills and experience while executing end-to-end algorithm development process of a unique platform aim to improve patients quality of life and survival.
Job description:
Execute statistical modeling and analysis of large data sets using ML and big-data algorithms
Perform end-to-end research and development of speech signal processing algorithms

We are looking for a Medical writer and Regulatory Affairs associate.
Primary function of the position:
Clinical scientific knowledge and writing skills to effectively and clearly communicate medical science information in writing. Generally, focus on either scientific medical writing, which includes clinical studies, and regulatory documents, scientific articles or marketing medical writing. Experience in regulatory aspects (RA), help to lead regulatory strategy and provide ongoing regulatory input.
Roles and Responsibilities:
Work with clinical teams and clients to understand the nature of the scientific work that they will be covering.
Assess data or products using medical expertise, and quickly develop expertise in new areas as needed for their writing.
Help to write studies for submissions to the FDA. The writing is also used in publications or medical journals, or for internal company use.
Comprehensive writing of clinical study reports, study protocols, annual reports, investigator brochures, risk/benefit analysis and integrated summaries from raw data.
Prepare abstracts, scientific exhibits, posters and verbal presentations.
Help with develop and write pharmaceutical training materials, eLearning content, video scripts, magazine articles, and presentations to be used by a variety of audiences.
Conduct comprehensive literature searches to enhance background understanding, and evaluate and analyze the information which will be written about.
Provide responses to regulatory agencies regarding product information or issues.
Maintain current knowledge of relevant regulations, including proposed and final rules. Help in manage activities such as audits, regulatory agency inspections etc.
Participate in the development or implementation of clinical trial protocols. Preparation and submission of regulatory agency applications, reports, or correspondence.
Provide regulatory guidance to departments or development project teams regarding design, development, evaluation, or marketing of products.

We are seeking an experienced antibody Scientist to facilitate our R&D efforts. As a key member of our multidisciplinary team, you will drive the discovery, design, and optimization of novel immunotherapy modalities using state-of-the-art computational, structural and biological methods.
Key Responsibilities:
* Implement cutting-edge structural methods, including molecular dynamics simulations, homology modelling and docking studies, to design antibody drug candidates.
* Harness AI/ML approaches and Antibody/Protein Engineering techniques to discover and optimize therapeutic antibodies.
* Stay updated with emerging technologies in structural biology and integrate novel approaches into our research programs to maintain our competitive edge.
* Appley molecular biology tools (Yeast display, Tissue culture, Flow cytometry, FPLC, HPLC, AKTA, ELISA, etc.) to produce and TEST antibodies in the lab.
* Collaborate closely with other laboratory personnel and CROs (Contract Research Organizations) to oversee antibody production, quality control, and efficacy testing.
* Contribute to project planning, scheduling, and cost estimation, ensuring timely and cost-effective delivery of assigned projects.
* Foster a culture of collaboration and excellence by building effective working relationships with colleagues, management, and external partners.

we are seeking a Research Assistant
Key Responsibilities:
Implementing and executing lab techniques in cell biology and media development.
Developing and standardizing cellular in-vitro assays.
Evaluating and adopting lab practices and methods.
Culture media preparation
Writing scientific reports and procedures and data presentations to other R&D teams.
Ability to collaborate effectively within a team and work independently.
Ability to work in a dynamic and fast-changing environment.
This full-time position is in the Science Park, Ness Ziona, Israel (not far from the Rehovot train station).