לוח משרות דרושים בוגרי מדעי החיים במרכז

We are a global bioagriculture company, leverages the natural power of
mycorrhizal fungi to improve the productivity, sustainability and profitability of commercial
agriculture and expand regenerative agriculture practices. 
We are the first to use innovative techniques to solve challenges inherent in high-volume mycorrhizal inoculant
production. We will not rest until every hectare of arable land is protected by mycorrhizae and every farmer benefits from higher crop yields while preserving our soils and permanently
sequestering carbon.
We are looking for a researcher with vast knowledge in soil microorganisms to play a key
role in our carbon sequestration project.
You Will Have an Opportunity to:
      Join an innovative company that is disrupting the bioagriculture market.
      Be a part of our leading R&D team. Directly contribute to the companys main growth engine.
Job Description:
      Strong literature research.
      Writing reviews, white papers, summaries and presentations.
       Plan and execute experiments according to the companys goals, timelines and work plans.
      Analysis, presentation, and implementation of findings and results.
      Develop and maintain protocols and operational processes.
      Study various soil microorganisms.
      Perform various soil tests.

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.