Clinical Laboratory Scientist

· Perform laboratory testing in compliance with PPFA policies, Title X, Federal and state licensing (CLIA and OSHA). Perform necessary duties to fulfill all testing requirements, from pre-analytical to analytical and post-analytical phases in a timely fashion.

· Perform DNA amplification tests, Rh testing, and testing for research, as needed.

· Report results to Planned Parenthood Mar Monte and other clinics.

· Answer phones, look up results, enter orders and results in LIS, answer clinic questions as capable and appropriate or refer questions to Laboratory Manager as needed.

· Assist Clinical Laboratory Manager to maintain adequate records for Quality Assurance, Quality Control, Proficiency Testing and other statistical data.

· Perform proficiency testing with strict adherence to CLIA guidelines (proficiency tests are treated no differently than patient samples).

· Follow corrective action procedures and documentation policies according to the Quality Assurance Plan.

· Maintain inventory of all lab supplies and reagents

 

· Works with/supervises volunteers/interns as appropriate.

· Perform other duties as assigned.

 

Ability to perform the duties described above. A typical means of acquiring those abilities would be:

· Current California Clinical Laboratory Scientist license (ASCP preferred)

· Two years of recent experience as a Clinical Laboratory Scientist in a clinical laboratory setting.

 

· Interface and communicate effectively with medical professionals, staff and the community

· Capable of identifying problems that may adversely affect test performance

· Self-motivated and capable of working independently

· Flexibility in working hours

· Strong organizational skills

· Support teamwork in the Laboratory