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Key Responsibilities and Required Skills for Virologist

💰 $70,000 - $150,000

Life SciencesResearchClinicalBiotechnology

🎯 Role Definition

A Virologist is an experienced life-sciences professional who designs, executes, interprets and communicates virology experiments and programs across discovery, translational research, clinical diagnostics, and product development. This role focuses on molecular virology, virus–host interactions, viral pathogenesis, assay development and validation (PCR, NGS, antigen/antibody assays), biosafety and regulatory compliance (BSL-2/BSL-3, GLP/GMP where applicable), and cross-functional collaboration with immunology, bioinformatics, clinical operations and regulatory affairs teams. The ideal candidate brings rigorous experimental design, robust data analysis, strong documentation practices, and the ability to translate complex virology findings into actionable program-level recommendations.


📈 Career Progression

Typical Career Path

Entry Point From:

  • Postdoctoral Fellow in Virology, Molecular Biology, or Microbiology
  • Senior Research Associate in Clinical or Industrial Virology
  • Clinical Laboratory Scientist with virology diagnostics experience

Advancement To:

  • Principal/Staff Virologist
  • Group Leader / Head of Virology
  • Director of Infectious Disease Research or Translational Sciences

Lateral Moves:

  • Molecular Diagnostics Lead
  • Viral Vector Development Scientist
  • Biosafety Officer / Laboratory Operations Manager

Core Responsibilities

Primary Functions

  • Lead the design, execution and interpretation of complex virology experiments to investigate viral replication, pathogenesis and virus–host interactions using molecular and cell-based approaches, translating results into clear scientific conclusions and project recommendations.
  • Develop, optimize and validate molecular diagnostic assays (qPCR/RT-qPCR, digital PCR, isothermal methods) and nucleic acid workflows for viral detection and quantification, producing validation reports, SOPs and performance-characteristic documentation for regulatory submission.
  • Plan and oversee next-generation sequencing (NGS) and metagenomic workflows for viral genome sequencing, variant analysis, and phylogenetics to support surveillance, strain characterization and downstream bioinformatics analyses.
  • Design and execute serology and immunoassay development (ELISA, multiplex bead assays, lateral flow prototypes) to measure antibody responses, neutralizing activity and correlate serological readouts with clinical endpoints.
  • Manage virus isolation, propagation and sample handling strategies in compliance with institutional biosafety requirements and BSL-2/BSL-3 practices, ensuring chain-of-custody and sample integrity without prescribing procedural steps.
  • Establish and implement rigorous assay qualification and validation plans, including defining acceptance criteria, statistical analysis of assay performance and generation of formal validation documentation to meet GLP/CLIA/GMP expectations.
  • Provide scientific oversight and technical mentorship to research associates, technicians and junior scientists; set experimental priorities, review data quality and ensure reproducible methods and documentation.
  • Collaborate with bioinformatics and data-science teams to integrate sequencing, PCR and serology data into interpretable visualizations, dashboards and program-level metrics that inform decision-making.
  • Design and run in vitro virology screens and cellular assays to evaluate antiviral compounds, neutralizing antibodies, vaccine candidates or host-targeted interventions, and present findings to cross-functional project teams.
  • Coordinate sample logistics, biobanking and cold-chain processes for clinical and preclinical specimens; define sample acceptance criteria, troubleshooting and sample processing standards to protect downstream analyses.
  • Prepare technical reports, regulatory submissions, manuscripts and IP filings; draft methods sections, materials lists and data summaries for peer-reviewed publication and patent applications.
  • Interface with clinical operations and study teams to design virology endpoints for clinical trials, support assay transfer to CLIA/GMP laboratories, and interpret virology data in the context of clinical outcomes.
  • Maintain and continuously improve laboratory quality management systems (QMS), including SOP authoring, training records, deviation investigations and corrective action plans to ensure audit readiness.
  • Lead cross-functional project meetings and act as the subject-matter expert for virology-related program decisions, timelines and resource allocations; translate scientific risk into program risk mitigation strategies.
  • Establish and monitor biosafety, waste management and personal protective equipment (PPE) policies for virology labs; coordinate required biosafety training, certifications and facility maintenance with institutional safety officers.
  • Evaluate and implement new technologies, instruments and reagents (droplet digital PCR, single-cell viral profiling, automated liquid handling) to accelerate throughput, sensitivity and reproducibility of virology workflows.
  • Manage laboratory budgets, reagent inventories and vendor relationships; negotiate service contracts for sequencing, peptide synthesis, antibody production and specialized assays.
  • Perform statistical analyses of assay and experimental data, generate confidence intervals and limits of detection, and synthesize results into actionable conclusions for R&D or diagnostic program advancement.
  • Lead or contribute to external collaborations and scientific partnerships with academic labs, CROs and public health agencies for surveillance, outbreak response or validation studies.
  • Provide technical input to regulatory and QA teams to ensure virology data packages meet country-specific regulatory expectations, and support responses to regulatory agency questions or audits.
  • Champion data reproducibility and FAIR data principles in virology datasets, ensure metadata standards for sequencing and clinical sample linking, and work with informatics to enable searchable, well-annotated data repositories.
  • Mentor and train internal stakeholders on interpretation of virology results for non-specialists (clinical, regulatory, commercial teams), translating complex virology concepts into clear, business-relevant language.

Secondary Functions

  • Support ad-hoc data requests and exploratory data analysis for cross-functional research or business planning.
  • Contribute to the organization's data strategy and roadmap by advising on virology-specific data requirements and integration points.
  • Collaborate with business units to translate data needs into engineering requirements for lab informatics, LIMS and analysis pipelines.
  • Participate in sprint planning and agile ceremonies within the data engineering and R&D teams to align experimental priorities with product development timelines.
  • Represent the organization at scientific conferences, workshops and stakeholder meetings; prepare presentations and poster materials highlighting virology program milestones.
  • Assist in hiring and onboarding virology staff, participating in candidate evaluations and training program design.

Required Skills & Competencies

Hard Skills (Technical)

  • Advanced knowledge of molecular virology techniques and concepts, including viral genome structure, replication cycles, and virus–host interactions as applied to experimental design and data interpretation.
  • Expertise in nucleic acid detection methods (RT-qPCR, qPCR, digital PCR) and assay development principles, including limit of detection, sensitivity, specificity and matrix effects.
  • Practical experience with next-generation sequencing (NGS) workflows for viral genomics, variant calling, consensus assembly and phylogenetic analyses.
  • Proficiency in serology and immunoassay development (ELISA, neutralization assays, multiplex platforms) and interpretation of humoral immune response data.
  • Working knowledge of biosafety and containment frameworks (BSL-2, BSL-3), biosafety risk assessment and laboratory compliance without providing procedural steps.
  • Familiarity with quality systems and regulatory environments (GLP, CLIA, GMP, FDA/EMA submissions) relevant to diagnostics, therapeutics or vaccine development.
  • Competence in cell culture models and in vitro infection assays for viral replication and antiviral testing, with emphasis on experimental design and biosafety oversight.
  • Experience with laboratory informatics systems, LIMS, sample tracking, and data management best practices, including metadata standards for sequencing datasets.
  • Basic bioinformatics skills or collaboration experience with bioinformaticians: command of common NGS analysis concepts, variant annotation, and data visualization.
  • Statistical literacy for assay validation and experimental analysis; experience using R, Python or equivalent tools for data analysis and visualization.
  • Ability to author reproducible technical documentation, SOPs, validation reports and peer-reviewed manuscripts.

Soft Skills

  • Strong scientific communication: able to distill complex virology results into clear written reports and concise slide presentations for technical and non-technical audiences.
  • Cross-functional collaboration mindset: experience working with clinical, regulatory, computational and commercial teams to drive programmatic goals.
  • Proven project management skills: planning experiments, tracking deliverables, managing timelines and coordinating external partners.
  • Critical thinking and problem-solving: rigorous approach to experimental design, troubleshooting and risk mitigation.
  • Mentorship and leadership: coaching junior scientists, providing constructive feedback and building high-performing laboratory teams.
  • Attention to detail and high standards for data integrity, reproducibility and documentation.
  • Adaptability and continuous learning: stays current with emerging virology methods, literature and technologies.
  • Ethical judgment and professionalism, including the ability to handle sensitive clinical or public-health data responsibly.

Education & Experience

Educational Background

Minimum Education:

  • MS in Virology, Microbiology, Molecular Biology, Immunology, or related life-science field, plus 3–5 years relevant virology experience; or
  • PhD in Virology, Microbiology, Molecular Biology, or related discipline (preferred for research leadership roles).

Preferred Education:

  • PhD with postdoctoral experience in molecular virology, antiviral development, viral immunology, or clinical virology.
  • Additional coursework or certification in biosafety, regulatory affairs, or clinical laboratory practice (e.g., CLIA).

Relevant Fields of Study:

  • Virology
  • Microbiology
  • Molecular Biology
  • Immunology
  • Biochemistry
  • Bioinformatics (for sequencing-focused roles)

Experience Requirements

Typical Experience Range:

  • 3–10+ years, depending on level (mid-level: 3–6 years; senior: 6–10+ years; principal: 10+ years)

Preferred:

  • Demonstrated track record developing and validating virology assays (molecular and/or serology), experience with NGS for viral genomics, and a history of collaborative contributions to translational or clinical programs. Experience working within regulated environments (GLP/CLIA/GMP) and managing BSL-2/BSL-3 laboratory operations is highly desirable.