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Key Responsibilities and Required Skills for Vaccine Research Director

💰 $220,000 - $350,000+

BiotechnologyPharmaceuticalsResearch & DevelopmentScientific LeadershipImmunologyVirology

🎯 Role Definition

The Vaccine Research Director is a senior scientific leadership role, acting as the strategic and technical cornerstone for the organization's entire vaccine discovery and early development pipeline. This individual is accountable for setting the scientific vision, guiding a multidisciplinary team of researchers, and driving the portfolio of vaccine candidates from initial concept through to successful IND submission. This role requires a blend of deep scientific expertise in immunology and virology, proven leadership in an industrial R&D setting, and the strategic acumen to navigate the complex scientific, regulatory, and business landscapes of vaccine development. The Director fosters a culture of innovation, scientific rigor, and urgency, ensuring the team is equipped and motivated to tackle emerging infectious diseases and unmet medical needs.


📈 Career Progression

Typical Career Path

Entry Point From:

  • Senior Principal Scientist, Immunology/Virology
  • Associate Director, Vaccine Research
  • Head of Preclinical Development

Advancement To:

  • Vice President, Research & Development
  • Chief Scientific Officer (CSO)
  • Head of Global Vaccine Development

Lateral Moves:

  • Director, Clinical Development (Biologics)
  • Director, Strategic Alliances & External Innovation
  • Director, Regulatory Affairs (Biologics)

Core Responsibilities

Primary Functions

  • Provide strategic scientific leadership and direction for all vaccine discovery and research programs, from target identification and validation through to lead candidate selection.
  • Develop and execute the long-term research strategy for the vaccine portfolio, ensuring alignment with corporate goals and the evolving public health landscape.
  • Lead, mentor, and manage a high-performing team of scientists and researchers, fostering their professional development and building a culture of collaboration, innovation, and scientific excellence.
  • Oversee the design, execution, and interpretation of critical in vitro and in vivo studies to evaluate vaccine immunogenicity, efficacy, and safety in relevant preclinical models.
  • Hold ultimate accountability for departmental budgets, resource allocation, and capital expenditures, ensuring efficient and effective use of resources to meet project goals.
  • Serve as the internal and external scientific subject matter expert for the organization's vaccine platform technologies and research programs.
  • Drive the seamless transition of vaccine candidates from the discovery phase into formal preclinical and early clinical development, ensuring a robust data package is prepared.
  • Author, review, and provide strategic input on key sections of regulatory submissions, including pre-IND meeting packages, Investigator's Brochures, and IND/CTA filings.
  • Establish and maintain a strong network of external collaborators, including academic institutions, government agencies (e.g., NIH, BARDA), and contract research organizations (CROs).
  • Champion the evaluation and integration of novel technologies, platforms, and methodologies to enhance the speed and success rate of vaccine discovery.
  • Lead cross-functional project teams, ensuring effective communication and alignment with colleagues in Clinical Development, Process Development, Manufacturing, and Regulatory Affairs.
  • Present research strategy, key data, and program updates to executive leadership, the Board of Directors, and scientific advisory boards.
  • Manage the intellectual property portfolio for the vaccine research pipeline, working closely with legal counsel to formulate patent strategies and file applications.
  • Ensure all research and laboratory activities are conducted in full compliance with internal standards and external regulations, including Good Laboratory Practice (GLP) where applicable.
  • Maintain a current and deep understanding of the competitive landscape, emerging scientific literature, and new therapeutic modalities in vaccinology.
  • Represent the company at major scientific conferences, publishing research in peer-reviewed journals and building the organization's scientific reputation.
  • Lead scientific due diligence for potential in-licensing opportunities, collaborations, and acquisitions to augment the internal pipeline.
  • Set clear, ambitious milestones and deliverables for all research projects and hold the team accountable for achieving them on time and within budget.
  • Develop and implement robust, scientifically sound assays for characterizing immune responses and determining vaccine potency.
  • Proactively identify and mitigate scientific and technical risks across the research portfolio, developing contingency plans to ensure program continuity.

Secondary Functions

  • Support ad-hoc data requests and deep-dive exploratory analysis for senior leadership and business development teams.
  • Contribute to the development and refinement of the organization's overarching R&D strategy and long-range roadmap.
  • Collaborate with business development and corporate strategy units to translate data and scientific insights into robust business cases for new programs.
  • Participate in and lead internal scientific review committees, governance bodies, and portfolio review meetings.

Required Skills & Competencies

Hard Skills (Technical)

  • Expertise in Vaccinology: Deep, authoritative knowledge of immunology, virology, and/or microbiology, specifically as it applies to vaccine design and immune response.
  • Vaccine Platform Experience: Hands-on experience and strategic understanding of modern vaccine platforms (e.g., mRNA, viral vector, protein subunit, VLP).
  • Preclinical Model Development: Proven ability to design, manage, and interpret data from relevant in vivo animal models for infectious diseases.
  • Regulatory Strategy: Strong working knowledge of the global regulatory landscape for vaccines, including FDA, EMA, and WHO guidelines for preclinical and early clinical development.
  • Assay Development & Qualification: Experience overseeing the development, validation, and implementation of a wide range of immunological and virological assays (e.g., neutralization assays, ELISpot, flow cytometry).
  • R&D Project Management: Proficiency in managing complex, multi-year research projects, including budget management, timeline tracking, and resource planning.
  • Scientific Writing and Data Analysis: Exceptional ability to author and critically review scientific documents, publications, and regulatory submissions.

Soft Skills

  • Strategic Leadership: The ability to craft a compelling scientific vision and motivate a team to execute on that vision, aligning research efforts with corporate objectives.
  • People Management & Mentorship: A demonstrated passion for developing talent, building effective teams, and leading through influence and direct management.
  • Executive Communication: Superb communication and presentation skills, capable of distilling complex scientific concepts for diverse audiences, from Ph.D. scientists to board members.
  • Cross-Functional Collaboration: A natural ability to build strong working relationships and drive consensus across different functional areas in a matrixed environment.
  • Problem-Solving & Critical Thinking: The capacity to analyze complex challenges, identify core issues, and develop innovative and pragmatic solutions.

Education & Experience

Educational Background

Minimum Education:

  • Ph.D. or M.D. in a relevant scientific discipline.

Preferred Education:

  • M.D./Ph.D. or a Ph.D. followed by significant postdoctoral research in a field directly related to vaccinology.

Relevant Fields of Study:

  • Immunology
  • Virology
  • Molecular Biology
  • Microbiology
  • Biomedical Sciences

Experience Requirements

Typical Experience Range:

  • 12-15+ years of relevant, post-doctoral experience in vaccine research and development.

Preferred:

  • A minimum of 8 years of direct experience within the biotechnology or pharmaceutical industry is strongly preferred. A proven track record of successfully advancing multiple vaccine candidates from discovery into preclinical or early clinical development is essential. At least 5 years of experience in a significant leadership role, including direct management and mentorship of Ph.D.-level scientists and research teams.