Molecular Virology Lead Scientist

Chenega MIOS$100K — $130K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Ph.D. in Virology, Microbiology, Immunology, or related field.
  • 7+ years in complex scientific research and study execution.
  • Proven experience in high-containment laboratory operations (BSL-2 to BSL-4).
  • Familiarity with FDA regulations and quality environments (GLP, GMP, GCP).
  • Experience with animal studies, including IACUC submissions and protocols.
  • Expertise in performing immunological assays (e.g., ELISA, flow cytometry).
  • Strong background in technical report and manuscript preparation.

Responsibilities

  • Conduct research to develop medical solutions for military-related viral diseases.
  • Design and oversee up to 15 animal studies annually, analyzing results post-execution.
  • Assist in writing IACUC animal protocols for research approval.
  • Perform various immunological assays to evaluate infection responses.
  • Prepare labs for regular safety and biosafety inspections.
  • Support grant writing efforts, aiming for at least three proposals per year.
  • Publish research findings in scientific journals and present at conferences.

Benefits

  • Comprehensive health, dental, and vision insurance.
  • Paid time off including holidays and vacation days.
  • Professional development opportunities.
  • 401(k) retirement plan with company match.
  • Flexibility for work-life balance.
  • Collaborative and innovative work environment.
  • Opportunities for travel related to scientific meetings.
Full Job Description
Overview

Chenega Services and Federal Solutions, LLC., a Chenega Professional Services' company, is looking for a Molecular Virology Lead Scientist to support research focused on the discovery and development of medical countermeasures targeting viral threats of military importance that require high-containment laboratory operations. The position supports research conducted in BSL-2, BSL-3, BSL-4, ABSL-2, ABSL-3, and ABSL-4 environments and requires working knowledge of FDA requirements related to Good Laboratory Practices, Good Manufacturing Practices, Good Clinical Practices, non-clinical research, clinical research, pivotal animal studies, and FDA Animal Rule-related activities. The incumbent will support Phase 1, Phase 2, Phase 3, and FDA Animal Rule studies, characterize medical products manufactured for clinical research, assist with study design and execution, support animal protocol development, conduct immunological assays, prepare technical reports and manuscripts, support funding proposal development, and maintain required CS-PRP and BPRP enrollment.

Responsibilities

  • Perform research aimed at the development of medical countermeasures to prevent and treat viral diseases of importance to the military. Research includes performing hands-on in vitrowork in BSL-2, BSL-3 and BSL-4 containment; and hands-on in vivo work in ABSL-2, ABSL-3, and ABSL-4 containment.
  • Assist in the design and development of research projects. Oversee the execution of approved research projects which can include up to ten (10) small animal studies and up to five (5) nonhuman primate studies per year. Will analyze the data from these studies, assist the PI in generation of reports, and assist in planning the next studies.
  • Assist the PI in the writing of animal protocols for submission and approval by the Institutional Animal Care and Use Committee.
  • Perform immunological assays to characterize responses to infection including, but not limited to, enzyme-linked immunoassay (ELISA), Western Blot, flow cytometry, plaque reduction neutralization test (PRNT) and immunohistochemistry (IHC).
  • Assist in the preparation of BSL-2, BSL-3, and BSL-4 labs for Safety, Bio-surety, CDC, and Department of Army Inspector General inspections at a minimum of 4 times a year. Use laboratory experience and expertise to provide training, perform laboratory supervisor duties and participate in laboratory containment working group(s) as needed to help ensure the labs, lab personnel, and procedures performed in the laboratory meet the applicable standards and regulations.
  • Assist PI in pursuit of funding from DTRA and other funding agencies in collaboration with the Government and USAMRIID to further the research portfolio of the Division and USAMRIID. Will assist with the preparation of a minimum of three (3) grants and proposals for prospective funding opportunities per year to the institute's portfolio management committee or equivalent for consideration.
  • Will prepare technical reports describing the status of projects to appropriate funding agencies. Frequency of delivery is quarterly or as defined by the reporting requirements of the department, division and funding sponsor.
  • Author manuscripts related to research findings and submit for publication in relevant scientific journals at least one manuscript per year. May be required to present work at Scientific Meetings (approximately 1-2 per year) which may require CONUS and OCONUS travel.
  • Develop or conduct annual reviews of SOPs for the Virology Division as assigned.
  • Provide the TPOC with a PI Technical Report NLT the last working day of each month.
  • Other duties as assigned


Qualifications

  • Ph.D. in Virology, Microbiology, Molecular Biology, Immunology, Biomedical Science, Infectious Disease, or a related scientific discipline.
  • Experience consistent with a Scientist 3-level role supporting complex scientific research, study execution, technical reporting, manuscript development, and high-containment laboratory operations.
  • Experience conducting or supporting viral disease, medical countermeasure, infectious disease, biodefense, or related biomedical research.
  • Experience supporting research conducted under FDA-regulated or quality-driven environments, including GLP, GMP, GCP, non-clinical research, clinical research, pivotal animal studies, or FDA Animal Rule-related activities.
  • Experience supporting Phase 1, Phase 2, Phase 3, FDA Animal Rule, or medical product characterization studies.
  • Experience designing, developing, executing, analyzing, and reporting scientific research projects.
  • Experience supporting animal studies, animal protocol development, and IACUC submission requirements.
  • Experience performing immunological assays such as ELISA, Western Blot, flow cytometry, PRNT, and immunohistochemistry.
  • Experience preparing technical reports, scientific manuscripts, SOPs, grants, proposals, and research documentation.
  • Experience providing training, laboratory supervisory support, or technical guidance in high-containment laboratory settings.
  • Ability to work in BSL-2, BSL-3, BSL-4, ABSL-2, ABSL-3, and ABSL-4 environments.
  • Ability to work with controlled substances.
  • Ability to obtain and maintain CS-PRP enrollment.
  • Ability to obtain and maintain BPRP enrollment.
  • Successfully pass background and drug screening


Preferred Qualifications:
  • Experience serving as a lead scientist or senior scientific contributor supporting virology, infectious disease, biodefense, or medical countermeasure programs.
  • Experience working in BSL-3 and/or BSL-4 laboratory environments.
  • Experience supporting ABSL-3 and/or ABSL-4 animal research studies.
  • Experience supporting FDA-regulated research, FDA Animal Rule studies, pivotal animal studies, or clinical product characterization efforts.
  • Experience preparing laboratories for Safety, Biosurety, CDC, or Department of the Army Inspector General inspections.
  • Experience preparing grant applications, research proposals, technical reports, and sponsor-facing documentation.
  • Experience authoring peer-reviewed manuscripts and presenting research findings at scientific conferences.
  • Experience developing or reviewing Virology Division SOPs.
  • Experience participating in laboratory containment working groups or performing laboratory supervisor duties.
  • Experience supporting DTRA or other government-funded research programs.


Knowledge, Skills and Abilities:
  • Advanced knowledge of molecular virology, viral disease research, infectious disease research, biodefense programs, and medical countermeasure development.
  • Knowledge of FDA non-clinical, clinical, pivotal animal study, GLP, GMP, GCP, and FDA Animal Rule-related research requirements.
  • Knowledge of BSL-2, BSL-3, BSL-4, ABSL-2, ABSL-3, and ABSL-4 laboratory operations and high-containment research requirements.
  • Knowledge of immunological assay methods, including ELISA, Western Blot, flow cytometry, PRNT, and immunohistochemistry.
  • Knowledge of animal study design, animal protocol development, IACUC submission processes, and study execution requirements.
  • Knowledge of laboratory inspection readiness, biosafety, biosurety, CDC inspection support, and Department of the Army Inspector General inspection preparation.
  • Ability to support research project design, study execution, data analysis, technical reporting, and follow-on study planning.
  • Ability to prepare technical reports, manuscripts, SOPs, grant materials, proposals, monthly reports, and scientific presentations.
  • Ability to provide training, laboratory supervisory support, and technical guidance to laboratory personnel.
  • Ability to communicate scientific findings clearly in written and oral formats to internal and external audiences.
  • Strong scientific judgment, analytical thinking, technical writing, organizational, leadership, and problem-solving skills.
  • Ability to work independently and collaboratively within multidisciplinary scientific research teams.

About Chenega MIOS

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Joining Chenega MIOS offers a unique opportunity to become part of an exceptional team of professionals operating in a variety of fields. This company is renowned for its commitment to innovation, leadership, and professional growth, making it a prime choice for those looking to advance their careers.

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Chenega MIOS is dedicated to fostering a workplace culture that values diversity and inclusion. Employees enjoy a comprehensive range of benefits designed to support both their professional and personal lives. From health and wellness programs to continuous learning and development opportunities, Chenega MIOS ensures that team members are well taken care of.

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For those beginning their career journey, Chenega MIOS offers internship programs that provide invaluable industry experience and exposure to real-world projects. Internships are a cornerstone of the company's commitment to nurturing new talent and equipping them with the necessary skills to excel.

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Career advancement is a key focus at Chenega MIOS. Employees are encouraged to engage in ongoing professional development through workshops, seminars, and diversity training. The company supports career progression through leadership training programs that prepare individuals for future roles within the company.

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