Clinical Laboratory Data Analyst (#0120) Singulex
THIS JOB HAS EXPIRED
Category: CV Monitoring
Summary
-A.M. Shift and P.M. Shift Available-
Description
Support the CLIA laboratory to ensure accurate and timely reporting of patient results.
Follow Standard Operating Procedures for data analysis and reporting of test results.
Organize test data for result approval and release by CLS personnel.
Meticulously analyze test data to identify outliers and anomalies for CLS personnel review.
Generate list of patient samples to be retested.
Document, trend and monitor performance metrics for the laboratory tests and reports on a daily basis utilizing current methods and enhancing new methods.
Organize and present performance metrics to the organization.
Follow Standard Operating Procedures for data analysis and reporting of test results.
Clerical skills (typing, FAX, excellent phone skills, copiers).
Utilize Laboratory Information System to investigate sample history.
Qualifications
BS in a biological science, or two years of experience as a Laboratory Assistant or Medical Technician involved in specimen handling, accessioning, and sample preparation in a high-volume setting.
Excellent typing and organizational skills, including Word, Excel, PowerPoint and Outlook, and has previous experience with at least one Laboratory Information System.
Must have excellent interpersonal skills, demonstrated ability to work effectively with multiple disciplines, good team approach, good written and oral communication skills, administrative skills, and above-average computer skills.
Work independently with minimal supervision.
Able to compile and accurately review large amount of laboratory data to identify outliers and anomalies.
Working knowledge of statistics, and outlier rejection algorithms.
Good documentation skills and attention to detail are essential.
Must have excellent written and verbal communication skills and the ability to understand, prepare, and communicate technical scientific information to a wide range of audiences.
Preferred Qualifications:
Two years experience operating FDA-approved, moderate-complexity tests on chemistry analyzers and at least one automated platform, such as TECAN.
2-5 years experience running and analyzing immunoassays, preferably in the regulated in-vitro diagnostic (IVD) or clinical laboratory industry.
Demonstrated experience with performing daily, weekly, and monthly analyzer maintenance.
Demonstrated experience utilizing quality control materials and documentation of quality control results. Capable of learning and using Westgard QC rules.
Strong understanding of GLP, QSR, and ISO regulatory requirements for IVD products.
Personal Characteristics:
Excellent cross-functional team participation skills.
Consistently displays a positive, patient attitude and extends respect and courtesy toward Supervisors and peers alike.
Highly organized and detail-oriented.
Results and goals oriented.
Excellent written and oral communication.
Ability to work in a fast-paced and changing environment; flexible and quickly adaptable to changing priorities.
Ability to inculcate the Singulex ?Top-5? core values and serve as positive example to team members and others within the organization.
Effective personal communication skills, shares knowledge with excellent training skills.
Having integrity and a strong work ethic.
Passionate for both personal and corporate success.
Ability to work with minimal supervision as a member of a team.
Commitment to quality.
Enthusiasm, attention to detail, the ability to meet aggressive deadlines, ability to think ?out of the box,? and ability to work effectively with others in a fast paced, highly-productive environment.
| Location: |
Alameda, CA
United States
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THIS JOB HAS EXPIRED