Location
West Sacramento, CA | United States
Job description
Our client's contribution to healthcare is offering a range of diagnostic solutions, clinical data management tools and process management expertise. Their goal is to provide solutions improving healthcare around the globe. They are part of a team of life science companies who are developing products that are paving the way in the fight to save lives.
If you are looking for an opportunity to contribute your skills and knowledge our client has an opportunity for a Clinical Scientist II.
- Support the Clinical Affairs team during Microbiology antimicrobial susceptibility testing (AST) clinical trials
- Responsible for electronic trial master file management
- Maintaining clinical trial documentation between sponsor and clinical trial sites
- Remote clinical site monitoring, including working directly with clinical trial sites to resolve issues
- Updating project lead(s) w/ data and any issues will be required
- Limited training of clinical trial personnel
- Troubleshooting instrument or data issues during the clinical trial
Salary: $DOE/ hr (long term contract)
Schedule: Monday Friday, 8am 5pm
Location: West Sacramento, CA
Benefits: Health Insurance Available Medical / Dental / Vision
Qualifications
- Bachelor's Degree -Life Science or related field w/ 2+ yrs of working experience in a laboratory
- OR Master's degree in Life Science or related field with 0-2 years of working experience.
- Knowledge of aseptic lab techniques, pipetting, good laboratory practice (GLP),
- Good Documentation Practices (GDP), and general wet bench experience
- Knowledge of good clinical practices (GCP)
- Skills to be successful - strong communication skills, ability to problem solve
- Ability to work in a multidisciplinary team environment
- Ability to be flexible and work in a rapidly changing task environment and w/ variety of tasks.
- Knowledge of electronic clinical trial master files
- Familiar w/ MS Office Work and Excel (simple formulas)
- Familiar w/ Florence Healthcare eTMF Software or similar A Plus!
- Ability to work onsite and/ or remotely (TBD)
- Ability to travel to sites as requested
- Must be authorized to work in the US for any employer
- The position is subject to passing a background check and drug screen
Keywords: clinical scientist, scientist, chemistry, GDP, manufacturing, quality, laboratory, data analysis, regulated industry, biological science, biochemistry, microbiology, immunoassay, lab, FDA, GMP, ISO, lean techniques, life science, wet bench experience, GLP
"By applying to this position, you are confirming that you understand the requirements needed for this position, and further confirm that you possess the necessary skills and requirements, as outlined above".
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