Overview
On Site
Hybrid
$40 - $55
Contract - W2
Contract - 2 Year(s)
Skills
clinical
research
quality control
Job Details
Our direct client (Leading BioPharmaceutical Company), is looking to hire a Clinical Research Associate (Quality Control) at Foster City, CA.
Long term contract
Open for either locations: Foster City CA or Santa Monica, CA
Description:
- Conduct Quality Control Analytical testing (e.g., ELISA, Flow Cytometry, PCR) of patient samples, stability samples, controls, and reagent qualification in a GMP environment.
- Assists in the training of QC staff as needed.
- Applies knowledge of current Good Manufacturing Practices (cGMPs) and Good Laboratory.
- Plan and successfully execute experiments and activities to support formulation and drug product process development work packages including molecular assessment, First-in-Human formulation development, Drug Product manufacturing process development, and clinical in-use evaluations.
- Clearly, timely, and accurately document data in appropriate repositories such as lab notebooks, reports, protocols etc
- Analyze, interpret, draw conclusion, and present or share data from experiments executed including preparation of appropriate documents such as reports and memos.
- Fully embrace a lean-agile mindset, matrix working environment, and continuous improvement
- Help support key project or department stakeholders as needed to ensure that company objects are met
- Use established data, reports and previous results to identify inappropriate variances and concerns as well as identity and report inconsistent results to manager or supervisor
- Participate in group meetings and efforts by presenting data or preparing information for others to present
- Support team initiative to drive business process excellence, scientific innovation, laboratory and work safety etc
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