לוח משרות דרושים ביולוגיה / בוטניקה

We are offering you to take a vital role in our research team that is responsible for constantly driving forward our ability to detect accessibility issues, enhancing the intelligence of our platform to provide customers with insights and usability enhancements that allow them to work more efficiently, and building innovative new products

To achieve those ends the team employs classic algorithms, data analysis, machine learning and generative AI.

You will be joining a team of highly professional and innovative engineers and scientists that are driven by passion for the domain and the mission of the company. We value scientific and engineering excellence, are committed to creating high impact products that reach our customers and work in collaboration with each other in an egoless environment.

Your Impact:
Research, design and implement new detection algorithms for web accessibility issues and improve existing ones.
Ensure all research is well documented and reproducible.
Build and enhance tools that enable data collection, labeling and analysis at scale for research purposes.
Integrate new models and algorithms into existing products.
Build interfaces for projects in the POC phase to enable demonstration and the collection of feedback from internal users and select design partners.

Were based in Tel Aviv, 5 minutes from Hashalom train station, and Yehudit light train station, and we have our own parking lot. We work in a hybrid mode, with flexible working hours.

we offer exciting career opportunities for those interested in joining a pioneering team that is committed to transforming cancer care for patients across the globe. Working at our cpmpany enables our employees to not only make a meaningful impact on the lives of patients, but to also learn and grow within a purpose driven environment. This is what we call the way its about how we work together, guided by our values, to give clinicians the insights they need to help patients make life-changing decisions.Our ValuesWe Seek A Better Way: We innovate boldly, learn from our setbacks, and are resilient in our pursuit to transform cancer careWe Make It Happen: We act with urgency, commit to quality, and bring fun to our hard workWe Are Stronger Together: We collaborate openly, seek to understand, and celebrate our winsWe Care Deeply: We embrace our differences, do the right thing, and encourage each otherThe PositionWe are looking for a Bioinformatics Scientist, experienced in high-throughput DNA data analysis and with a strong interest in genomics and algorithm development. The successful candidate will provide support for analysis of large and complex genomics data sets related to cancer and will empower, through the specific domain knowledge and experience, the various aspects related to the research and development of our tools and products.An essential role of this position is to engineer, in collaboration with R&D and production team members, high-quality tools for genomic sequence data analysis while adhering to our state of the art software engineering methodologies. The bioinformatician will create novel tools, customize existing and third-party tools to implement new or improve existing applications of our products.The successful candidate will be an essential team player in the effort for significant optimization of our growing genomic data analytic platform. This entails working cross-functionally with data scientists, clinical analysts, software engineers, and business analysts to ensure our genomic data becomes a powerful asset and value growth driver. Specifically, the candidate will participate in the design and prototyping of processing pipelines and algorithms for analysis of the genetic data to improve clinical performance and to optimize the entire system to shorten the processing times and costs. The ideal candidate will have the ability to see the big picture, understand user needs and requirements, and identify the opportunities for applying solutions from bioinformatics, algorithms, and data science domains.This is a remote position based out of our Israel office. ResponsibilitiesAnalyze next-generation high-throughput DNA sequencing data ranging from single research experiments to very large data setsDevelop tools and automated analysis pipelines for bioinformatics analyses, diagnostic tests, including variant detection and quality control Design new algorithms, methods and tools for DNA sequencing data analysis and propose improvements to the existing research infrastructure Produce high quality written documentation including study plans and reports Produce correct conclusions based on rigorous mathematical analysis and principles of statistics and probability Collaborate effectively with R&D, production, and clinical teams to build efficient workflows Be the "go to" person for bioinformatics and related issues Ensure internal processes and metrics are aligned to create the highest product quality and competitive advantage Develop Python software infrastructure to support algorithm testing and simulation studies Produce clear, concise and correct technical documentation including research reports and algorithm specifications

Looking for a Temporary Lab Technician (Maternity Leave Replacement)!
Join my professional NGS lab with a great atmosphere.

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