UCSF
Location
San Francisco, California
Quantitate drug concentrations for HIV, TB, and other substances in biological specimens using LC/MS/MS analytical methods. Responsibilities include sample preparation, instrument calibration, data interpretation, and maintaining regulatory compliance with FDA and NIH guidelines.
Requires a BA/BS degree in a related science or an equivalent combination of education and experience. Candidates should possess basic scientific laboratory techniques and proficiency in Microsoft Office software.
The purpose of this position is to quantitate drug concentrations for anti-human immunodeficiency virus (HIV) and anti-tuberculosis (TB) medications, antibiotics, and controlled substances primarily in human hair, dried blood spot (DBS), and urine samples (but may include other biological specimens, such as whole blood, plasma, serum, nail, saliva, etc.), utilizing high-performance liquid chromatography (HPLC)-tandem mass spectrometry (LC/MS/MS) analytical methods for pharmacokinetic, compliance, and efficacy studies. Laboratory duties include, but not limited to, logging in samples via a laboratory data management system (LDMS); sample preparation; operating and calibrating analytical instruments; using and calibrating micropipettes; thorough documentation in lab books, log books, and paperwork; and the actual analysis (and subsequent interpretation) of data. The successful candidate will also assist in the validation of LC/MS/MS methods for antiretroviral and anti-TB drug analysis in hair, but may also include other biological specimens, in compliance with the Food and Drug Administration’s (FDA’s) Good Laboratory Practice (GLP) and National Institute of Health’s (NIH’s) Division of AIDS’ (DAIDS) Clinical Pharmacology Quality Assurance (CPQA) regulatory guidelines.
The UCSF Hair Analytical Laboratory (HAL) analyzes antiretroviral, anti-tuberculosis (anti-TB), antibiotic, and controlled substance concentrations in hair (but may include other biological specimens such as urine, dried blood spot (DBS), plasma, serum, whole blood, nail, saliva, etc.) in the context of HIV and TB prevention and treatment studies using assays that are developed and validated according to the Federal Food and Drug Administration’s (FDA’s) guidelines for bioanalytical methods and the National Institute of Health’s (NIH’s) Division of AIDS’ (DAIDS) Clinical Pharmacology Quality Assurance Program (CPQA). This position is responsible for overseeing and maintaining high-quality regulatory functions in the laboratory.
This HAL Staff Research Associate I position will assist senior analysts in determining drug concentrations in samples utilizing validated high-performance liquid chromatographic (HPLC)-tandem mass spectrometric (LC-MS/MS) bioanalytical methods.
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