Microphysiological Systems Associate Study Director

4 weeks ago

Frederick, Maryland, United States Laulima Government Solutions Full time
Job Description

Lauded as a leading government service provider, Laulima Government Solutions is seeking a highly skilled Microphysiological Systems Associate Study Director to join our esteemed team. As a key member of our research team, you will be responsible for conducting collaborative research projects on microphysiological systems within the outlined government program or collaborating with other Study Directors on projects or programs under the guidance of leadership.

Key Responsibilities:

  • Conducts collaborative research projects on microphysiological systems within the outlined government program or collaborates with other Study Directors on projects or programs under the guidance of leadership.
  • Efficiently plans, executes, and reports scientific activities conducted in accordance with directives from the Virology Branch.
  • Works with research leadership to conduct research involving infectious diseases caused by Tier 1 viruses, Risk Group 4 viruses, and uncommon viruses.

Research areas include, but are not limited to:

  • Microphysiological systems including, but not limited to organ-chips, organoids, 3D bioprinted setups, and other complex, 3-dimensional in vitro systems
  • Reverse genetics and genomics
  • Viral life cycle surrogate systems (e.g., viral pseudotyping, VLPs, minigenome and budding systems)
  • Gene knock-in/knock-out studies
  • Mechanisms-of-action studies
  • Enzymatic assays
  • Animal experiments
  • Virology assays including, but not limited to, TCID50 and plaque assay
  • DNA/RNA extraction, purification, quantification, transcription, replication, amplification, and mutagenesis, RT-PCR/real-time PCR, microarray

Additional Responsibilities:

  • Analysis of viral load in blood and tissue samples using quantitative real time PCR (one-step and two-step assays)
  • Generate master and working stocks of virus and other microbial agents as directed that are well documented and characterized.
  • Generate study plans using approved templates and SharePoint processes provided prior to initiation of in vitro and in vivo experiments.
  • Generate high quality interim and final study reports and develop them for timely publication in peer reviewed journals.
  • Actively participate in practices/processes to enhance data quality and integrity including periodic review of study execution to identify gaps and refine procedures.
  • Supervise more junior staff members in effectively conducting and troubleshooting assays, analyzing and reporting results.
  • Develop and implement training and cross-training programs to assure continuity of operations and scientific core and screening activities.
  • Develop and revise Standard Operating Procedures (SOPs) and methods for laboratory operations.

Requirements:

  • Minimum of a Doctorate (PhD, DVM or MD) in Virology or a related field from an accredited college or university.
  • Must have hands-on laboratory experience with and working knowledge of microphysiological systems as documented by a strong publication record.
  • Must have proven experience and a publication record in conducting virus experiments using organ-chips and/or organoid models.
  • Working knowledge of quality assurance and quality control systems, such as Good Laboratory Practices (GLP).
  • Excellent communication skills with team members and rapport with leadership, and agility to integrate within a diverse team of scientists and non-scientists.
  • Must be able to pivot to changing priorities as directed by government and contract leadership.
  • Must have four (4) years' specialized training and research.
  • Ability to obtain/maintain DoJ Security Risk Assessment (SRA) approval.
  • Must be willing to participate in periodic drug screening.
  • Must have the ability to obtain/maintain certification in Chemical Personnel Reliability Program and/or Biological Personnel Reliability Program.
  • Must have the ability to obtain/maintain CDC Select Agent Program approval.
  • Ability to work under BSL-4 conditions. Able to wear respiratory protection.

Preferred Qualifications:

  • Experience with viral Select Agents is highly desired.
  • Proficiency in Word, Excel, and PowerPoint.
  • Basic understanding of laboratory information management systems (LIMS).
  • Demonstrate interpersonal, oral and written communication, and organizational skills.
  • Demonstrate ability to ability to work independently, design experiments, and analyze data.

Clearance Requirements:

  • Active Secret clearance. (Individual must be able to meet the requirements for T3 level investigation.)

We are an Equal Opportunity/Affirmative Action Employer. We are proud to state that we do not discriminate in employment decisions based on race, color, religion, sex, pregnancy, sexual orientation, gender identity, national origin, age, protected veteran status, or disability status.

If you are a person with a disability and you need an accommodation during the application process, please click here to request accommodation.

We E-Verify all employees.

The Alaka`ina Foundation Family of Companies (FOCs) is comprised of industry-recognized government service firms designated as Native Hawaiian Organization (NHO)-owned and 8(a) certified businesses.

The Family of Companies (FOCs) includes Ke`aki Technologies, Laulima Government Solutions, Kpono Government Services, and Kapili Services, Po`okela Solutions, Kkaha Solutions, LLC, and Pololei Solutions, LLC.

Alaka`ina Foundation activities principally benefit the youth of Hawaii through charitable efforts which includes providing innovative educational programs that combine leadership, science & technology, and environmental stewardship.

For additional information, please visit #ALAHP #LI-JS1 #ClearanceJobs

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