Job description
Under supervision, the Staff Research Associate(SRA) typically performs a wide variety of standard repetitive procedures without detailed technical supervision, usually in a well-established occupational field (i.e., chemistry, microbiology, etc.). They may also modify, vary or adapt standard procedures to meet the needs of research projects or improve unsatisfactory tests, and after studying available literature, analyze and alter conditions under which determinations are made. They may also acquire and apply a body of knowledge and skill in a field of comparatively narrow scope where the emphasis is on specialized techniques
This HAL Staff Research Associate II position will assist senior analysts and train and mentor junior analysts to determine drug concentrations in samples utilizing validated high-performance liquid chromatographic (HPLC)-tandem mass spectrometric (LC/MS/MS) bioanalytical methods.
The purpose of this position is to design, develop, and execute a variety of analytical methods to quantitate antiretroviral, anti-TB, and antibiotic drugs and possibly controlled substances using liquid chromatography-tandem mass spectrometry (LC/MS/MS), primarily in hair samples (but may include other biological specimens, such as urine, dried blood spot, plasma, serum, whole blood, nail, saliva, etc.), for pharmacokinetic, compliance, and efficacy studies. Techniques may include, but are not limited to, protein precipitation, liquid-liquid extraction (LLE), and solid phase extraction (SPE). The successful candidate will have some knowledge and engage in analytical LC/MS/MS method development, validation, and the assaying of clinical samples in compliance with 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.
In addition, will also be required to prepare Standard Operating Procedures (SOPs) and Analytical Validation Reports (AVR) for submission to Clinical Pharmacology Quality Assurance (CPQA); respond to inquiries from CPQA; train and mentor new staff members after successfully completing and understanding internal laboratory SOPs; operate and calibrate analytical instruments; use and calibrate micropipettes; prepare, analyze, run, and interpret data; and thoroughly document in lab books, log books, and paperwork.
To see the salary range for this position (we recommend that you make a note of the job code and use that to look up): TCS Non-Academic Titles Search (ucop.edu)
Please note: The compensation ranges listed online for roles not covered by a bargaining unit agreement are very wide, however a job offer will typically fall in the range of 80% - 120% of the established mid-point. An offer will take into consideration the experience of the final candidate AND the current salary level of individuals working at UCSF in a similar role.
For roles covered by a bargaining unit agreement, there will be specific rules about where a new hire would be placed on the range.
To learn more about the benefits of working at UCSF, including total compensation, please visit: https://ucnet.universityofcalifornia.edu/compensation-and-benefits/index.html
Department Description
The Division’s work is featured frequently in the media, and it is often visited by international, national, state and local dignitaries and delegations. The Division consists of approximately 36 faculty members and 140 academic and staff employees. It is the largest Division of the Department of Medicine (DOM) at ZFGH, with a total expenditure budget of approximately $45 million dollars
Required Qualifications
- BA/BS in a related science including one year of recent/directly related work experience following degree completion, utilizing techniques or methods required by the position and demonstrating technical expertise in these areas; or an equivalent combination of education and experience
- One year related scientific techniques and procedures as learned from academic laboratory or experimental field experience, especially utilizing LC-MS/MS systems (preferably Micromass Quattro Ultima (MassLynx software), Sciex API 5000 (Analyst software), and/or Agilent 6495 (MassHunter software) and HPLC systems
- Demonstrate reliability, organizational skills, attention to detail, and record-keeping abilities based on prior experience
- Strong basic laboratory techniques such as micropipetting; measuring solutions using volumetric flasks, graduated cylinders; making reagents, mobile phases, and standard solutions; using centrifuges, vortexes, and other equipment in an analytical laboratory
- Outstanding communication skills
Computer software skills (MS Word, Excel and PowerPoint)
Preferred Qualifications
- One year of Laboratory Data Management System (LDMS) experience
- Prior knowledge in FDA Good Laboratory Practices (GLP) and NIH DAIDS Clinical
- Knowledge of the basic principles in chemistry
- Strong lab book preparation and documentation skills
- Pharmacology Quality Assurance (CPQA) regulations
About UCSF
Pride Values
In addition to our PRIDE values, UCSF is committed to equity – both in how we deliver care as well as our workforce. We are committed to building a broadly diverse community, nurturing a culture that is welcoming and supportive, and engaging diverse ideas for the provision of culturally competent education, discovery, and patient care. Additional information about UCSF is available at diversity.ucsf.edu
Join us to find a rewarding career contributing to improving healthcare worldwide.
Equal Employment Opportunity
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