Clinical Scientist II
3 weeks ago
Location: West Sacramento, CA
Pay rate: $63 Hourly.
Duration: 12+ Months (Possible Extensions)
Job Description:
- The Clinical Affairs Scientist I will support the Clinical Affairs team during Microbiology antimicrobial susceptibility testing (AST) clinical trials. The incumbent performs testing as defined and planned by supervisor; Prepare for clinical trial studies by selecting organisms for clinical trial testing and sub-culturing microorganisms.
- Assist with the coordination of clinical study materials including the receipt, ordering, distribution, tracking, and shipment to clinical sites.
- Updating project lead(s) with data and any issues will be required, as well as an ability to work in cross-functional teams.
Position Requirements:
- 2+ years’ experience in laboratory experience. Strong communication skills with the ability to work in a multidisciplinary team environment.
- Ability to problem solve is a must. Knowledge of aseptic lab techniques, pipetting, good laboratory practice (GLP), good documentation practices (GDP), and general wet bench experience.
- Ability to be flexible and work in a rapidly changing task environment and with variety of tasks. Familiarity with Excel and data analysis is desired.
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Clinical Scientist II
3 weeks ago
West Sacramento, United States TechDigital Corporation Full timeDescription/Comment: The Clinical Affairs Scientist P2 will support the Clinical Affairs team during Microbiology antimicrobial susceptibility testing (AST) clinical trials. Working under a Clinical project lead, the incumbent will be interacting with cross functional teams and responsible for clinical trial site support, including but not limited to lead...
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Clinical Scientist II
3 weeks ago
West Sacramento, United States TechDigital Corporation Full timeThe Clinical Affairs Scientist P2 will support the Clinical Affairs team during Microbiology antimicrobial susceptibility testing (AST) clinical trials. Working under a Clinical project lead, the incumbent will be interacting with cross functional teams and responsible for electronic trial master file management; maintaining clinical trial documentation...
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