Salzman Group is seeking organic chemists to join our team of scientists in a drug development biotechnology laboratory in Katzrin, in the Golan Heights. The successful candidate will perform chemical synthesis in various transformations and purifications as well as analytical testing and analysis of data.
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BSc or MSc in Chemistry
Experience desired with Organic Synthesis
Experience with analytical techniques including; HPLC, FTIR, GC-MS, UV-Vis
Ability to work both independently and in a team environment.
Salzman Group Ltd. is an Israeli biotechnology firm focused on the discovery and development of transformative pharmaceuticals. We are seeking QC Analysts to join our analytical laboratory in Katzrin, Golan Heights, Israel.
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B.Sc. or M.Sc., in analytical or organic chemistry or chemical engineer
Analytical laboratory experience in HPLC, LC/MS, GC/MS etc.
Knowledge of GLP/GMP requirements
Knowledge in development and validation of analytical methods
Fluent in English and Hebrew
Good computer skills for technical writing and data analysis
Salzman Group Ltd. is expanding and is looking for an experienced Clinical Research Associate (Level II/III) to join our Clinical Operations department.
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3 years’ experience as a CRA previously employed by a CRO or Pharmaceutical company (mandatory)
Full knowledge with ICH-GCP guidelines, valid GCP training certificate from the last year (mandatory)
CRA training certified
Bachelor’s degree minimum in any of the Bio-Medical/Paramedical fields
Previous therapeutic field experience in oncology – an advantage
Ability to monitor Clinical Study sites independenly in Hospitals mainly within the center of Israel, (mandatory)
High level English
Strong interpersonal-relationship skills and a team player
Ability to act and think out of the box
Willing to learn and grow
Full-time, CRA position available to work within our Phase I-IV Clinical Operations Team. The CRA will be involved in all clinical trial aspects with a focus on sites in Israel. Possibility for home-based position as well.
As a CRA, you will manage all aspects of study site monitoring according to SOPs, GCP, and ICH guidelines, including pre-study qualification and initiation visits, routine monitoring, close-out of clinical sites, and maintenance of study files.
CVs should be sent via e-mail to: firstname.lastname@example.org