The ideal candidate will be responsible performing lab activities in accordance with applicable Methods, Plans, SOPs/SWPs, GLP regulatory guidelines and 21 CFR Part 11 as directed from Group Leader and Sr. Analysts. Independently conduct Bio-analysis validation and sample analysis in support of nonclinical and clinical studies. Conduct Pre-Study with minimal supervision. Utilize establish techniques to compile and analyze data. Document work and maintain study documentation and lab records.
Responsibilities
- Understand and comply with GLP requirements and follow Methods, Plans and SOP/SWPs and related lab procedures; comply with safety policies, comply with company policies.
- Use and properly maintain lab instrument and equipment appropriately for assigned tasks.
- Conduct Bio-analysis validation and sample analysis independently meeting company quality standards.
- Conduct pre-study method development with minimal supervision.
- Prepare worksheets.
- Data processing and table preparation (i.e., QC data and preparation, data integration, raw data printing, preparation of chromatograms for the report, use of Watson LIMS, etc.)
- Maintain accurate records of work and study documentation per Good Documentation Practices as per company SOPs.
Qualifications
- Bachelor's degree or equivalent experience
- ELISA – absorbance, fluorescence, luminescence
Research Analyst (LBA) in Hoffman Estates at CMIC, Inc.
This position is listed as full time and onsite. It was posted 2 days ago.