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We are looking for a Chemistry Researcher Temp position.
What will you do?
Lead research, lab and printing activity experiments
Develop new products
Support existing products
Track, document, analyze and present results

the innovation arm of the Sheba Medical Center. With the vision of redesigning healthcare by 2030 we are collaborating with the various stakeholders' communities in the local and global ecosystem to achieve it. A central community we engage with is the startup community. The engagement with this community is focused on two avenues: The first is the formulation of the partnerships in a way that maximizes the opportunity and value for all involved (the company, clinicians, Sheba). The second is the management of the community of startups that are under the umbrella and creating value that supports the success and growth of the companies in their developmental, regulatory, clinical, and financial trajectories. 
Role responsibility as part of the Startup unit:
Managing the entire evaluation, negotiation, and onboarding process of the best companies into
Main Responsibilities:  
Leading the collaboration formation of startup companies with and Sheba in terms of all involved parties: startups, clinicians, and Sheba.
Managing the commercial negotiation and legal processes with companies while maximizing the opportunity and creating a win-win.
Leading and executing the active efforts in order to achieve goal of recruiting the best companies:
Mapping and identifying the needs and gaps at Sheba and the network that require a technological solution.
Scouting for the most suitable and best solutions and companies in the local and global market (as relevant).
Proactively approaching the selected companies and striving to create interest and partnership aligned with the needs and the involved clinicians.
Support and consulting regarding the maintenance of existing agreements - renewal, update, etc.

We are looking for a skilled and driven Experiment Operator to join our team.
As an Experiment Operator, your role will be examining and interpreting extensive datasets in order to derive valuable insights and offer actionable solutions.
You will have the opportunity to work both independently and collaboratively in a variety of testing environments, such as laboratories and outdoor settings.
It is expected that you display proficiency in operating multiple devices efficiently.
Additionally, your contribution will be valuable in creating test plans and reports to effectively manage and organize test data.

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