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Director Preclinical Development Jobs in Seattle, WA

... in preclinical development. Jade was launched based on assets licensed from Paragon Therapeutics ... Role Overview The Director, Clinical Operations will oversee the strategic and operational ...

The Senior Director, Biomarkers, Immunology is an independent leader with wide-reaching scientific ... sites, including PreClinical Sciences (PCS), Research, Translational, Clinical Development ...

Senior Medical Director

Seattle, WA · On-site

$270K - $333K/yr

Contribute to the clinical development strategy, including indication selection, trial design, and ... Collaborate closely with translational medicine, preclinical, and regulatory teams to align ...

Senior Medical Director

Seattle, WA · On-site

$270K - $333K/yr

Contribute to the clinical development strategy, including indication selection, trial design, and ... Collaborate closely with translational medicine, preclinical, and regulatory teams to align ...

Senior Medical Director

Seattle, WA · On-site

$270K - $333K/yr

Contribute to the clinical development strategy, including indication selection, trial design, and ... Collaborate closely with translational medicine, preclinical, and regulatory teams to align ...

Director, Protein Engineering

Redmond, WA · On-site

$180K - $240K/yr

SystImmune has a robust preclinical pipeline of potential cancer therapeutics in the discover and ... development. We offer an opportunity for you to learn and grow while making significant ...

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Showing results 1-20

Director Preclinical Development information

See Seattle, WA salary details

$46.1K

$105.1K

$176.4K

How much do director preclinical development jobs pay per year?

As of Sep 6, 2026, the average yearly pay for director preclinical development in Seattle, WA is $105,137.00, according to ZipRecruiter salary data. Most workers in this role earn between $79,700.00 and $123,500.00 per year, depending on experience, location, and employer.

What is a director preclinical development?

A Director of Preclinical Development oversees the early-stage research and testing of drug candidates before they enter clinical trials. They manage preclinical studies, ensuring regulatory compliance, safety, and efficacy assessments. This role involves coordinating with cross-functional teams, external partners, and regulatory agencies to advance promising compounds. Strong expertise in toxicology, pharmacology, and regulatory guidelines is essential. The director plays a key role in shaping the preclinical strategy to support successful drug development.

What are the typical responsibilities and team dynamics for a director preclinical development?

A Director of Preclinical Development is responsible for overseeing the planning, execution, and management of preclinical research programs, ensuring that studies meet scientific, regulatory, and project milestones. You will typically work with cross-functional teams including toxicologists, pharmacologists, regulatory affairs professionals, and external partners, fostering collaboration throughout the drug development process. The role often involves reviewing study designs and data, preparing regulatory submissions, and providing strategic direction to advance compounds toward clinical testing. Working closely with upper management, you'll play a key part in shaping research priorities and resource allocation. This position offers significant influence over drug development strategies and opportunities for advancement to higher executive or scientific leadership roles.

What are the key skills and qualifications needed to thrive in the director preclinical development position, and why are they important?

To thrive as a Director Preclinical Development, you need deep expertise in pharmaceutical or biotechnology research, strong project management abilities, and an advanced degree (Ph.D., Pharm.D., or equivalent) in a life sciences field. Familiarity with regulatory guidelines (such as GLP), experience using data management and statistical analysis software, and prior leadership roles in preclinical studies are essential. Exceptional communication, problem-solving, and team leadership skills set candidates apart in managing multidisciplinary teams and collaborative projects. These competencies are crucial for successfully guiding drug candidates through preclinical stages while ensuring regulatory compliance and timely project delivery.

What are popular job titles related to Director Preclinical Development jobs in Seattle, WA?

For Director Preclinical Development jobs in Seattle, WA, the most frequently searched job titles are:

What job categories do people searching Director Preclinical Development jobs in Seattle, WA look for?

The top searched job categories for Director Preclinical Development jobs in Seattle, WA are:

Infographic showing various Director Preclinical Development job openings in Seattle, WA as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 15% Part Time, and 3% Contract. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution, with an average salary of $105,137 per year, or $50.5 per hour.

Executive Director / Vice President, Discovery / Research (Seattle)

Work In Biotech

Seattle, WA • On-site

Full-time

Re-posted 4 days ago


Job description

Executive Director / Vice President, Discovery / Research

Confidential Search: Executive Director / Vice President, Discovery/Research

Location: Seattle, WA (Hybrid)

Company: Stealth-mode biotechnology venture

Position Summary

A stealth‑mode biotechnology company in Seattle is seeking an accomplished Executive Director or Vice President of Discovery/Research to lead scientific strategy and execution across discovery, preclinical research, and IND‑enabling development for a pipeline of prophylactic monoclonal antibodies targeting viral pathogens.

This executive will serve as the scientific head of research, setting the long‑term discovery vision while ensuring near‑term execution of the company’s lead program through IND. The role demands strong leadership, strategic insight, and deep subject‑matter expertise, paired with a willingness to operate hands‑on within a small, stealth startup environment.

This is a rare opportunity to shape the foundational scientific platform, build a high‑caliber discovery capability, and directly influence value creation at a critical early stage.

Key Responsibilities Strategic Leadership of Discovery & Research
  • Define and articulate the scientific vision for discovery and preclinical research in alignment with company mission and long‑term pipeline goals.
  • Build a differentiated discovery strategy for prophylactic monoclonal antibodies, including target selection, mechanistic prioritization, and candidate profiling.
  • Create an integrated scientific plan that supports both innovation (new platform capabilities, viral target‑space expansion) and execution (lead optimization and IND readiness).
Ownership of IND‑Enabling Research Strategy
  • Serve as the executive scientific leader responsible for aligning discovery research with the critical path to IND and beyond, ensuring all research outputs support regulatory expectations and development timelines.
  • Oversee integration of virology, pharmacology, structural/biophysical characterization, PK/PD, nonclinical safety, and CMC considerations into a coherent development plan.
  • Lead senior‑level interactions with regulatory consultants and contribute to IND strategy, scientific narrative, data interpretation, and responses to regulatory authorities.
Leadership of Scientific Functions (Internal & External)
  • Build and lead a high‑performing research organization, initially through strategic use of CROs, contractors, and academic partnerships, with selective internal hiring over time.
  • Mentor and develop scientific staff; instill a culture of rigor, creativity, accountability, and translational thinking.
  • Drive cross‑functional alignment across research, CMC, clinical strategy, and operations—without reliance on large internal departments.
Virology, Pharmacology & Mechanistic Research Oversight
  • Guide experimental strategy for virology and pharmacology, including in vitro and in vivo models, neutralization assays, and mechanistic studies required for candidate differentiation.
  • Ensure that research activities support translational hypotheses, dose selection strategies, and safety margins.
Structural & Biophysical Characterization Strategy
  • Direct structural and biophysical studies (cryo‑EM, crystallography, SPR/BLI, epitope mapping) that inform antibody engineering, lead selection, and regulatory justification of mechanism.
  • Integrate structural insights into overall discovery strategy and development decision‑making.
External Partnerships & Scientific Representation
  • Serve as the senior scientific representative in relationships with CROs, academic collaborators, industry partners, and scientific advisors.
  • Represent the company’s research strategy in board discussions, investor interactions, and scientific forums as appropriate.
Organizational & Operational Leadership in a Lean Environment
  • Establish research operating principles, quality standards, and data‑review processes suited to a small but high‑ambition company.
  • Manage budgets, timelines, and strategic resourcing to maximize scientific productivity in a lean setting.
Qualifications Required
  • Ph.D. in Virology, Immunology, Molecular Biology, Structural Biology, Pharmacology, or a related field.
  • 15+ years of relevant industry experience with increasing leadership responsibility; prior role(s) at Executive Director, VP, or equivalent strongly preferred.
  • Proven track record directing monoclonal antibody discovery and optimization from concept through preclinical development and to BLA.
  • Experience leading programs toward IND‑enabling studies and partnering on IND strategy.
  • Deep scientific expertise in at least one of: viral pathogenesis, virology and antiviral pharmacology, antibody engineering, structural biology, or translational sciences.
  • Demonstrated ability to build, mentor, and lead scientific teams—preferably in early‑stage or resource‑constrained environments.
  • Exceptional ability to manage external partners and drive execution across multiple disciplines.
  • Strong communication skills, including the ability to represent scientific strategy to executives, boards, and external stakeholders.
Preferred
  • Experience with prophylactic or infectious disease–focused antibody programsli>
  • Prior involvement in company formation, platform development, or early pipeline strategy.
  • Experience interacting directly with the FDA or other global health authorities.
  • Proven track record of establishing research capabilities and scientific culture in start‑up or lean environments.
Why This Role?
  • Executive‑level influence on strategy, scientific direction, and pipeline creation.
  • Opportunity to build and lead the research function at a formative moment.
  • Ability to directly shape the path to IND for the lead antibody program.
  • High‑impact, mission‑driven work with competitive compensation and meaningful equity ownership.
Seniority level
  • Executive
Employment type
  • Full‑time
Job function
  • Business Development and Sales
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