Research Associate I - ACVP

Research Associate I - ACVP

Job
Employee Type: exempt full-time
Division: AIDS & Cancer Virus Program
Facility:
Frederick:
Ft Detrick

Location:

PO Box B, Frederick, MD 21702 USA

The Frederick National Laboratory is operated by Leidos Biomedical Research, Inc. The lab addresses some of the most urgent and intractable problems in the biomedical sciences in cancer and AIDS, drug development and first-in-human clinical trials, applications of nanotechnology in medicine, and rapid response to emerging threats of infectious diseases.
Accountability, Compassion, Collaboration, Dedication, Integrity and Versatility; it's the FNL way.

The AIDS and Cancer Virus Program (ACVP) is an integrated, multidisciplinary program that pursues basic and applied studies aimed at improving our understanding of AIDS-associated viruses, including studies intended to facilitate the improved diagnosis, prevention and treatment of HIV infection and AIDS, and AIDS related tumors, particularly those associated with other viruses such as KSHV. The Program consists of several independent but highly interactive research Sections headed by Principal Investigators, whose work spans from fundamental molecular virology through in vitro studies, to in vivo studies in non-human primate (NHP) models, to international viral epidemiology.

The ACVP also has Research Support Core Groups (Cores) that provide critical and often unique technical support capabilities to ACVP laboratories and other laboratories within the NCI, NIH, and to extramural investigators.

ACVP is looking for a Research Associate I to join the dynamic and collaborative group under the leadership of Dr. Denise Whitby in the Viral Oncology Section (VOS) within the AIDS and Cancer Virus Program. Our laboratory has unique expertise in conducting international molecular and immunologic/epidemiologic studies of infection with Kaposi’s sarcoma-associated herpes virus (KSHV) and other oncogenic viruses, along with basic studies of KSHV biology and laboratory testing, including CLIA certified testing, in support of clinical research on KSHV.

The Research Associate I will perform laboratory testing and specimen processing in support of CLIA-regulated activities, research studies,and collaborative projects.

• Receive, accession, label,process, aliquot, store, retrieve, and ship human biospecimens whilemaintaining accurate specimen identity and traceability.
• Process whole blood for separation of plasma, PBMCs, as well as oral fluid, effusions, CSF, tissues,and other OPIM.
• Perform established molecular,(quantitative real time PCR) and if needed serologic, and cell based laboratoryprocedures according to approved SOPs and if applicable, regulatory requirements.
• Maintain complete, accurate,and contemporaneous laboratory records, including specimen logs, assayworksheets, instrument records, reagent records, and electronic databases.
• Perform routinequality-control activities and document assay performance, control results,deviations, corrective actions, and other required quality records.
• Identify specimen, assay,equipment, or documentation issues and promptly communicate concerns tosupervisory or senior laboratory staff.
• Perform minimal routine maintenance and calibration of laboratory equipment, including function checks,N2 replenishment, thawing, temperature monitoring, and documentation of saidmaintenance activities.
• Monitor reagent and supply inventories, track expiration dates and lot numbers, and assist with ordering and restocking.
• Support cell cultureactivities, including maintenance of cell lines and preparation of cells for laboratory assays.
• Enter, review, and organizelaboratory data using FMPro databases, and Microsoft Office applications.
• Coordinate work across multiple concurrent studies and prioritize time-sensitive specimen processing and testing activities.
• Participate in laboratorytraining, competency assessment, proficiency testing, audits, and continuous quality-improvement activities.
• Perform other relatedlaboratory and administrative duties as assigned, working collaboratively withother VOS staff and external investigators to support study goals,…