לוח משרות דרושים מדעי החיים, טבע וחקלאות משרה מלאה

We are seeking a highly motivated and experienced M.Sc.-level researcher to join our Biochemistry R&D team. The selected candidate will play a key role in the development of innovative multi-bodies and contribute to advancing our technology platform. This is a maternity leave replacement for one year! Responsibilities:
* Design and execution of various assays to characterize binding, mode of action and calibration for pharmacokinetics analysis assays.
*  data analysis, documentation, and presentation of scientific and experimental work.
* Meeting project goals and timelines. Hands-on Experience:
* Cell culture techniques, including sterile practices with various cell types and maintenance of mammalian cell lines (advantageous)
* Surface plasmon resonance (advantageous)
* HPLC experience with different chromatography techniques (advantageous) Qualifications:
* M.Sc. degree in life sciences with relevant lab experience (must)

We are a leading-edge company that designs multi-specific human antibodies, is seeking a Procurement Manager to own and elevate our end-to-end sourcing function. Youll partner with suppliers, vendors, and cross-functional teams to implement strategic procurement processes that drive cost savings, ensure supply-chain resilience, and support our R&D and Operational goals. Position Overview: Were seeking a strategic, detail-driven procurement leader with a proven track record of building sourcing functions from the ground up. You will design and execute our end-to-end procure-to-pay process, negotiate and manage key supplier relationships across both direct (R&D, manufacturing, operations) and indirect (IT, facilities, services) spend categories, securing all mission-critical goods and services on time and within budget. This hands-on role offers full ownership today-and the mandate to hire and lead a team as we scale. Exceptional negotiation, analytical, and cross-functional communication skills are a must.
Responsibilities: Define, Build & Implement Processes: Architect and deploy scalable procure-to-pay workflows-from requirements gathering through PO issuance, receipt, and invoice reconciliation-across direct and indirect spend. Strategic Sourcing & Cost Savings: Develop category-specific sourcing strategies; negotiate agreements; onboard and qualify alternative vendors to drive redundancy and deliver measurable savings. Technology & Systems Solutions: Evaluate, design, and implement procurement platforms, reporting dashboards, and integrations ( ERP /P2P/ BI ) to automate workflows and enable Real-Time spend visibility. Cross-Functional Requirements Translation: Partner with R&D, IT, Finance and operations to translate project needs into clear, actionable sourcing specifications and SLAs. Supplier Relationship Management: Own supplier selection, performance tracking, risk mitigation, and contract lifecycle management for all critical goods and services. Compliance & Reporting: Ensure adherence to quality/regulatory standards and internal policies; produce KPIs, spend analyses, and executive-level dashboards to drive informed decision-making.

We are a leading biotech company that uses Machine Learning and AI technologies to create superior drugs for cancer and autoimmune disorders by programming antibodies to become dynamic functional switches that affect biology in new ways. We are seeking a motivated researcher to join one of our leading programs as a key player in the drug discovery department and contribute to the discovery of novel therapeutics. As an R&D project researcher, you will implement protein engineering methodologies and contribute to the establishment and implementation of in-vitro antibody characterization using cell-based assays.

we are a global publicly-traded commercial-stage oncology company developing a profoundly different cancer treatment therapy called tumor treating fields (TTFields) for patients with solid tumors. TTFields therapy is a non-invasive, novel, antimitotic treatment modality that utilizes proprietary technology attempting to slow or reverse tumor progression by inducing tumor cell death.
our company's commercialized product, Optune, is approved for the treatment of adult patients with glioblastoma (GBM) in the USA, Europe, and Israel.
our company has ongoing or completed clinical trials and is further expanding its efforts into several other solid tumor indications - non-small cell lung cancer, pancreatic cancer, and other types of solid cancers.
We are looking for a Researcher the biology research team in the preclinical department. As a Researcher you will be part of basic scientific research for the identification of the responses to electric fields in the molecular and cellular levels.
This is a full time position in our R&D center, Haifa, Israel, and reported to the
Senior Scientist.
ESSENTIAL DUTIES AND RESPONSIBILITIES:
Effective experimental planning, preparation of protocols, conductance of experiments according to protocol, documentation of the results, interpretation of the results and preparation of a summary report in accordance with the highest scientific standards
Must be highly detail oriented and very well organized
Responsible for performing in vitro experiments according to good laboratory practice
Maintain personal and other employees safety.

we are a global publicly-traded commercial-stage oncology company developing a profoundly different cancer treatment therapy called tumor treating fields (TTFields) for patients with solid tumors. TTFields therapy is a non-invasive, novel, antimitotic treatment modality that utilizes proprietary technology attempting to slow or reverse tumor progression by inducing tumor cell death.
our company's commercialized product, Optune, is approved for the treatment of adult patients with glioblastoma (GBM) in the USA, Europe, and Israel.
We are looking for Biostatistics for our Biostatistics team.
As a biostatistician, you will contribute to the statistical aspects of our clinical trials.
The role will involve the usage and implementation of statistical techniques commonly used for Oncology clinical trials.
In addition, the role will include clinical SAS programming for data verification.
This is a full time, Hybrid position as part of our team in Isarel.
ESSENTIAL DUTIES AND RESPONSIBILITIES:
Contribute to protocol development in conjugation with clinical development and operation teams and responsible to assess the feasibility of the study endpoints and develop the Statistical Analysis Plan (SAP)
Report the study results in the Clinical Study Report (CSR)
Oversight of the CRO and validate other vendors' statistical activities
Assist to provide statistical advice and advice on statistical aspects of clinical and preclinical projects
Approve statistical outputs: Table, Listing and Figures (TLFs) and the analysis datasets produced by the statistical programming team using SAS
Work within a multidisciplinary team and serve as a point of contact between clinical operation, CRO and SAS programmer within the statistical department
Provide statistical input to the study-related documents: study execution plans (including Data Management Plan), eCRF design and Edit Checks specifications, eCRF completion guidelines, data reconciliation plans
Review SAS coding and specifications
Other responsibilities as assigned.