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Genomic Characterization Scientist Security Clearance

Job in Frederick, Frederick County, Maryland, 21701, USA
Listing for: Keaki Technologies
Per diem position
Listed on 2026-01-01
Job specializations:
  • Research/Development
    Research Scientist, Clinical Research
Job Description & How to Apply Below
Position: Genomic Characterization Scientist with Security Clearance
The Alaka`ina Foundation Family of Companies (FOCs) has a potential need for a Genomic Characterization Scientist to support our government customer located in Fort Detrick, Frederick, MD. DESCRIPTION OF RESPONSIBILITIES:
* Perform molecular protocols and technologies to identify microbiological pathogens, characterize pathogenesis mechanisms of BSATs and study the host immune response.

* Provide expertise in epitope mapping on polyclonal humoral responses to pathogen using phage domain programmable arrays, B cell receptor (BCR) repertoire characterization in vaccinated or infected animals or human subjects, and advanced Immunological concepts.

* Development and improvement of animal model important for BSATs. Characterization of animal species genomic background (e.g. MHC expression), development and species-specific reagents, and comparative genomic to evaluate the model compared with humans. Generation of agnostic tools to evaluate the animal model and human samples with the same assays.

* Prepare or contribute to technical reports and manuscripts for publication, publicly present data upon request. Assist in the establishment of extramural collaborations and contracts to augment the research program. Show understanding of the progress toward publication to include their efforts to obtain and format data and research methods, within a reasonable timeframe suitable for that research project and given support.

A Lab Progress Report should be submitted monthly. An acceptable alternative format than publication outlines is contribution to Quarterly Reports to funding agencies. Update Lab Data weekly in a shared continuity folder for all publications/Quarterly Reports that includes all supporting data or directories where data is stored (raw and processed data and sample processing records).

* Oversee the technical work of supporting personnel assigned to the research programs. Specifically, to train and ensure SOPs, sample and analytical workflows are followed, tracked, and documented by supporting personnel. Data records are maintained in a current status within reasonable timeframe after sample and analytic processing. Lab Data Records and SOPs are updated upon change with a full description of the change and signature of the PI.

Lab SOPs are reviewed and signed semi-annually.

* Maintain laboratory records documenting sample processing, protocol design and usage, and data management that meet current CGS and Institutional requirements and ensure continuity and collective sharing of resources. Communicate to the PI or assigned supervisor(s) experimental data, laboratory issues or other work- related issues. Workflows and SOPs shall be reviewed and signed on a semi-annual basis or as determined by CGS before being implemented.

* Assist in maintaining laboratory equipment, specimens and reagents inventories, as well as keeping an organized, safe and professional work environment.

* Under special circumstances, may be required to work variable work schedules (second shift) and occasional weekends in order to accomplish time sensitive laboratory tasks.

* Participate in all activities pertinent to lab performance and safety, including weekly lab clean-up to avoid contaminations, be primary, secondary or tertiary point of contact for equipment and/or laboratory spaces (POC will be contacted by phone during emergencies, such as alarms or loss of power, and need to respond according to emergency plan for the CGS). Contact commercial company and/or USAMRIID medical maintenance, Clinical Engineering (CEB) when an instrument is malfunctioning or needs periodical PM, and escort engineers during the scheduled visit(s) ure reagents in the lab are not expired and ordered periodically to avoid shortage in reagents and stops in processes.

Maintain reagent, sample, and intermediary processes products inventory updated and stored in the designated areas, following biosafety guidance's and CGS protocols. Receive and appropriately storage reagents and samples delivered to the CGS. REQUIRED DEGREE/

EDUCATION/CERTIFICATION:

M.S. in biology, biochemistry or microbiology REQUIRED

SKILLS AND EXPERIENCE:

* Four (4) years'…
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