לוח משרות דרושים בוגרי מדעי החיים משרה מלאה

The internship program provides learning experience, mentoring and valuable work experience in the field of clinical trials. We provide our interns the opportunity to work on meaningful assignments and make sure that they gain real world experiences (in the areas of Regulatory & Finance and Supply & CRA support).

This program provides comprehensive trial and site administration experience. Under the oversight of the COM Lead/COMs and CTCs, the person prepares, collates, distributes and archives clinical documents. The Interns supports clinical supply & non-clinical supply management and ensures timely maintenance of tracking and reporting tools, as applicable.

* Internship duration up to 12 months *

Responsibilities:
Trial and site administration:
Track (e.g. essential documents) and report (e.g. Safety Reports).
Ensure collation and distribution of study tools and documents.
Update clinical trial databases (CTMS) and trackers.
Clinical supply & non-clinical supply management, in collaboration with other country roles.
Manage Labeling requirements and coordinate/sign translation change request.
Document management:
Prepare documents and correspondence.
Collate, distribute/ship, and archive clinical documents, e.g. eTMF.
Assist with eTMF reconciliation.
Execute eTMF Quality Control Plan.
Update manuals/documents (e.g., patient diaries, instructions).
Document proper destruction of clinical supplies.
Prepare Investigator trial file binders.
Obtain translations of documents.
Regulatory & Site Start-Up responsibilities: Collaborate with other country roles to:
In a timely manner, provide to and collect from investigators forms/lists for site evaluation/validation, site start-up and submissions.
Obtain, track and update study insurance certificates.
Support preparation of submission package for IRB/ERC and support regulatory agencies submissions.
Publish study results for GCTO and RA where required per local legislation.

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.