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Kerr Dental

Director, Nonclinical Safety Assessment Expert – Multiple Therapeutic Areas

Kerr Dental

Director overseeing nonclinical safety assessments for drug development. Leading interdisciplinary teams and engaging with global Health Authorities for regulatory compliance.

Posted 6/18/2026full-timeSan Diego • California • 🇺🇸 United StatesLead💰 $185,500 - $344,500 per yearWebsite

About the role

Key responsibilities & impact
  • Provide global, end to end nonclinical safety leadership across multiple therapeutic areas and modalities.
  • Serve as the primary Preclinical Safety (PCS) authority on cross functional R&D teams and in interactions with global Health Authorities.
  • Lead PCS Target Teams to design, integrate, interpret, and apply nonclinical safety assessment programs.
  • Represent Preclinical Safety on cross functional R&D project teams.
  • Define and implement fit for purpose, modality appropriate nonclinical programs in collaboration with PCS and external line functions.
  • Lead global Health Authority interactions, including negotiation on safety issues and scientific interpretation.
  • Author nonclinical safety sections of internal and regulatory documents.
  • Drive and coordinate communication strategies between PCS and R&D project teams.
  • Mentor and coach colleagues on drug development strategy.

Requirements

What you’ll need
  • Advanced scientific degree (PhD, MD, DVM, PharmD, or equivalent) in Toxicology, Pharmacology, or related discipline; or DABT; or equivalent industry experience.
  • 5 plus years of experience as a nonclinical safety Project Team member, preferably across multiple development phases up to registration.
  • 8 or more years of experience in nonclinical drug development (e.g., project toxicologist, pharmacologist, study director).
  • Demonstrated expertise across multiple modalities (e.g., small molecules, biotherapeutics, oligonucleotides) and their safety considerations.
  • Proven track record of direct interaction with global Health Authorities, including shaping regulatory strategy and submission writing.
  • Recognized scientific and regulatory expertise in nonclinical safety assessment within a global drug development context.
  • Demonstrated leadership and influence in complex, matrix managed, international project environments.
  • Strong problem solving capability in multidisciplinary, project driven settings.

Benefits

Comp & perks
  • Health insurance
  • Life insurance
  • Disability benefits
  • 401(k) with company contribution and match
  • Generous time off package including vacation, personal days, holidays and other leaves
  • Performance-based cash incentive
  • Eligibility for annual equity awards

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools
nonclinical safety assessmenttoxicologypharmacologydrug developmentregulatory strategysubmission writingsafety assessment programsproject toxicologistbiotherapeuticssmall molecules
Soft Skills
leadershipmentoringcoachingproblem solvingcommunicationinfluencecollaborationnegotiationstrategic thinkingteam coordination
Certifications
PhDMDDVMPharmDDABT