Top 22 Associate director Jobs in Oxnard, Ca

Associate Director of Toxicology, Small Molecules
Kelly Services —Thousand Oaks, CA
- $200,000 - $230,000 a year
- Full-time
- Doctor of Philosophy
- US work authorization
- Fair chance
- Paid holidays
- Disability insurance
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Associate Director, Continuous Improvement
Glass House Brands, Inc. —Camarillo, CA
- $110,000 - $140,000 a year
- Full-time
- Spanish
- 7 years
- Writing skills
Associate Director Field Effectiveness
Amgen —Thousand Oaks, CA
- $137,814.75 - $186,455.25 a year
- Doctoral degree
- Office
- Master's degree
- Disability insurance
- Health insurance
Associate Director - Information Systems
Amgen —Thousand Oaks, CA
- $171,556.35 - $232,105.65 a year
- Computer science
- Doctoral degree
- Computer Science
- Disability insurance
- Health insurance
4d
Associate Director - Business Operations Partner - Rheumatology and Nephrology
Amgen —Thousand Oaks, CA
- $151,074.75 - $204,395.25 a year
- Doctoral degree
- 5 years
- Master's degree
- Disability insurance
- Health insurance
12d
Associate Director, Consumer Marketing
MannKind Corporation —Westlake Village, CA
- $148,000 - $222,000 a year
- Management
- 3 years
- Analysis skills
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10d
Associate Director Process Development
Amgen —Thousand Oaks, CA
- $164,021.95 - $221,912.05 a year
- 3 years
- Master's degree
- High school diploma or GED
- Disability insurance
- Health insurance
Associate Director Global Clinical Program
Amgen —Thousand Oaks, CA
- Remote
- Management
- Doctoral degree
- 3 years
- Disability insurance
- Health insurance
19h
Associate Director, Global Insights, General Medicine
Amgen —Thousand Oaks, CA
- $180,447.35 - $244,134.65 a year
- Doctoral degree
- Office
- Master's degree
- Disability insurance
- Health insurance
Associate Director, Finance, – Revenue & Reporting
Sage —Thousand Oaks, CA
- $160,000 - $190,000 a year
- Remote
- CPA
- Bachelor of Science
- Writing skills
- Health insurance
- Dental insurance
Value and Access Insights Associate Director, Obesity
Amgen —Thousand Oaks, CA
- $170,719.95 - $230,974.05 a year
- Doctoral degree
- 5 years
- Office
- Disability insurance
- Health insurance
Associate Director, Regulatory Affairs - Advertising/Promotion
MannKind Corporation —Westlake Village, CA
- $148,000 - $222,000 a year
- 5 years
- Master's degree
- Bachelor's degree
Quick Apply
12d
Associate Director, Commercial Data Science
Amgen —Thousand Oaks, CA
- $176,985.30 - $239,450.70 a year
- Azure
- Doctoral degree
- Office
- Disability insurance
- Health insurance
Obesity Forecasting, Associate Director
Amgen —Thousand Oaks, CA
- Doctoral degree
- 3 years
- Master's degree
- Disability insurance
- Health insurance
13d
Associate Director, Orchestration Engine
Amgen —Thousand Oaks, CA
- $150,768.75 - $203,981.25 a year
- Doctoral degree
- Office
- 3 years
- Disability insurance
- Health insurance
CD&A - Associate Director, Agentic AI Business Solutions
Amgen —Thousand Oaks, CA
- $150,858.85 - $204,103.15 a year
- Hybrid work
- 7 years
- Doctoral degree
- Master's degree
- Disability insurance
- Health insurance

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Associate Director of Toxicology, Small Molecules

Kelly Services -
Thousand Oaks, CA

Quick Apply

Job Details

Full-time
$200,000 - $230,000 a year

Benefits

Paid holidays
Disability insurance
Health insurance
Dental insurance
Vision insurance
Retirement plan
Paid sick time

Qualifications

Data integrity assurance
FDA submissions
Research design
GLP
Data integrity and documentation
Pre-clinical study projects
ICH guidelines
Clinical research compliance
Doctor of Philosophy
Data quality monitoring
Compliance documentation
Data-driven problem-solving
Regulatory submission editing and review
Communication with regulatory authorities for clinical trials
Safety and toxicology data reporting
Toxicology research projects

Full Job Description

Kelly® Science & Clinical is seeking an Associate Director of Toxicology opportunity with one of our clients, a clinical-stage biopharmaceutical company in the Los Angeles, CA area seeking to redefine pain management. If you are driven by the prospect of translating cutting-edge scientific discoveries into tangible advancements and are poised to advance your career, join us as we pioneer progress in the biotechnology industry.
Workplace: Hybrid in the Los Angeles, CA or San Francisco, CA areas
Position Title: Associate Director of Toxicology
Salary range: 200,000-230,000/year
About the Company
Join one of the leading clinical-stage biopharmaceutical innovators dedicated to redefining pain management through next-generation, non-opioid therapies. With a culture grounded in scientific rigor, patient-centered innovation, and a track record of executive success, we’re seeking talented individuals to transform care for patients living with pain-related conditions. Our team operates at the forefront of breakthrough science in an environment that values creativity, collaboration, and the advancement of meaningful therapeutics.
Associate Director, Nonclinical Safety (Toxicology)
Are you passionate about advancing innovative therapeutics through strategic toxicology leadership? We are seeking an accomplished and driven Associate Director of Toxicology to shape and deliver nonclinical safety strategies that will enable transformative discovery and development programs. This is a high-impact, visible role—perfect for a scientific leader eager to influence program direction across a dynamic portfolio.
Position Highlights
The Associate Director will serve as the principal nonclinical safety/toxicology expert within multidisciplinary teams, driving the strategic design, execution, and interpretation of integrated safety data pivotal to candidate selection and late-stage advancement. You will blend scientific depth with operational acumen, ensuring the highest standards of data integrity, risk assessment, and regulatory alignment.
Key Responsibilities
Strategic Leadership & Program Influence

Act as primary toxicology expert on cross-functional teams, shaping nonclinical safety strategies from early discovery through clinical development.
Synthesize and contextualize nonclinical findings to support robust risk-benefit assessments and go/no-go decisions.
Drive candidate selection and portfolio prioritization through deep scientific insight and collaborative partnership.

Study Design & Operational Excellence

Lead the design, oversight, and monitoring of exploratory (non-GLP) and IND-enabling GLP toxicology and safety pharmacology studies, as well as post-IND investigations (e.g., sub-chronic, chronic, reproductive, carcinogenicity studies).
Provide scientific oversight for CROs and external partners, ensuring rigorous execution, high-quality data, and GLP/ICH compliance.
Proactively address data gaps and implement mitigation strategies in fast-evolving development contexts.

Data Analysis & Program Communication

Critically analyze and interpret complex nonclinical safety data, translating findings into actionable recommendations for drug development teams and executive stakeholders.
Present data and strategy with clarity and authority to internal governance bodies and project teams.

Regulatory Strategy & Compliance

Author and review nonclinical sections of key regulatory documents (INDs, IBs, briefing books, responses to agencies), ensuring clarity, completeness, and alignment with global regulatory expectations.
Partner with Regulatory Affairs to drive successful health authority interactions (e.g., FDA), maintaining up-to-date knowledge of guidances and requirements.
Ensure full compliance with GLP, ICH, and other applicable guidelines.

Cross-functional Partnership

Collaborate closely with Discovery, DMPK, Clinical Pharmacology, Clinical Development, and Regulatory teams to deliver seamless and coherent development programs.
Contribute scientific expertise to integrated project plans and portfolio decision-making.

Qualifications

Ph.D. in Toxicology, Pharmacology, or related discipline (DABT highly preferred)
~10+ years of industry experience in nonclinical safety/toxicology, with a demonstrated record of advancing small molecule drug development candidates
Deep expertise in the design, monitoring, and interpretation of GLP and non-GLP safety studies supporting IND-enabling and late-stage development
Command of GLP/ICH regulations and regulatory toxicology strategy
Proven experience authoring regulatory submissions and engaging directly with health authorities
Experience managing CRO relationships and driving data quality in externalized study settings
Background in pain, neuroscience, or related therapeutic areas is advantageous
Prior work in early-stage biotech or high-growth R&D environments preferred

Attributes for Success

Exceptional scientific judgment, analytical rigor, and creative problem-solving
Skilled communicator with a talent for translating complex data into impactful strategy and recommendations
Collaborative, proactive, and highly organized—adept at thriving in cross-functional, fast-paced teams

#P1

As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Please note: The following benefits reflect Kelly's general offerings. Eligibility may vary by assignment, location, and job type. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan.

Why Kelly® Science & Clinical?

Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world’s most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals-it’s the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed.

About Kelly

Work changes everything. And at Kelly, we’re obsessed with where it can take you. To us, it’s about more than simply accepting your next job opportunity. It’s the fuel that powers every next step of your life. It’s the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life-just ask the 300,000 people we employ each year.

Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California’s state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.

Kelly may use AI-powered tools during the recruitment and hiring process. For full details, including how Kelly uses AI, your rights, and how to request a reasonable accommodation, visit the Recruitment Artificial Intelligence Notice.

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associate director jobs in oxnard, ca

Associate Director of Toxicology, Small Molecules

Associate Director, Continuous Improvement

Associate Director Field Effectiveness

Associate Director - Information Systems

Associate Director - Business Operations Partner - Rheumatology and Nephrology

Associate Director, Consumer Marketing

Associate Director Process Development

Associate Director Global Clinical Program

Associate Director, Global Insights, General Medicine

Associate Director, Finance, – Revenue & Reporting

Value and Access Insights Associate Director, Obesity

Associate Director, Regulatory Affairs - Advertising/Promotion

Associate Director, Commercial Data Science

Obesity Forecasting, Associate Director

Associate Director, Orchestration Engine

CD&A - Associate Director, Agentic AI Business Solutions

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