Executive Director, Toxicology
Job in
San Diego, San Diego County, California, 92101, USA
Listed on 2026-07-01
Listing for:
Clinical Dynamix
Full Time
position Listed on 2026-07-01
Job specializations:
-
Research/Development
Job Description & How to Apply Below
Executive Director, Toxicology
Do you have a Toxicology background and strong leadership? Our Publicly Traded Client is expanding. Looking for an Executive Director, Toxicology with strong leadership experience. Company is based in San Diego and does require on-site presence. Robust compensation package offered including full relocation and other long term incentives.
Essential Functions
- Provides leadership, mentorship, and oversight to the Toxicology function in their conduct of all nonclinical safety assessments for Company's discovery and development compounds
- Drives the strategic vision and direction of the Toxicology function at Company to enable development of world-class capabilities in support of numerous small molecule and biologic modalities
- Works in collaboration with other Research and Development Team members and with Company leadership to ensure safety pharmacology and toxicology support is provided to ensure provision of requisite data in a timely manner to meet development goals.
- Critically evaluate toxicology results and provides timely strategic advice to project teams and senior management on the potential impact of toxicology results on Program and Clinical/Regulatory strategy
- Oversee and provide direction in the preparation of Safety Pharmacology and Toxicology sections of regulatory documents (IND, CTA, NDA, briefing books, Investigator Brochures, etc.)
- Represent Preclinical Development on discovery and development-stage program teams
- Develops critical insights from data summaries and shapes presentations of results to peers, colleagues and Company Management.
- Oversees the adherence to all SOPs for Toxicology.
- Proactively research and stay current on all applicable regulatory guidances
- Other duties as assigned
Knowledge and Qualifications
- Common Knowledge &
Skills: - Acts as a "trusted advisor" across the company and may be recognized as an external expert
- Provides strategy, vision and direction regarding issues that may have company-wide impact
- Requires in-depth knowledge of the functional area, business strategies, and the company's goals
- Possesses industry-leading knowledge of Toxicology assessment of small molecules and biologics
- Must be self-motivated, detail-oriented, decisive
- Ability to quickly learn and think independently
- Excellent interpersonal & communication skills with the ability to interact professionally and effectively with peers, management, and leadership both within and outside the Company
- Excellent managerial skills and experience fostering career development of direct and indirect reports
- Demonstrated ability to influence and lead others.
- Job Specific Knowledge &
Qualifications: - Extensive knowledge of toxicologic pathology is beneficial
- Extensive knowledge of managing clinical Contract Research Organizations (CRO's)
- Demonstrated involvement in the preparation of INDs, CTAs, NDAs, and MAAs
- Maintains broad knowledge of scientific principles and theories and possesses intellectual mastery of multiple scientific areas
Typical Experience or Education
- PhD in Toxicology, Pathology or closely related discipline and 12+ years of pharmaceutical/biotech experience, including managing clinical Contract Research Organizations. Experience in toxicologic pathology is beneficial
- D.V.M and 8+ years of similar experience noted above. Extensive previous leadership experiences also required
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