Top 85 Senior associate director Jobs in Carlsbad, Ca

Associate Director of Toxicology
Kelly Services —Carlsbad, CA
- $175,000 - $250,000 a year
- Full-time
- Master's degree
- Doctor of Philosophy
- Neurology
- Paid holidays
- Disability insurance
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Senior Director, Business Transformation
Thermo Fisher Scientific —Carlsbad, CA
- $212,000 - $317,975 a year
- Full-time
- 6 years
- Office
- Bachelor's degree
- Commuter assistance
- Paid parental leave
Associate Director of Construction & Maintenance - San Diego Zoo Safari Park
San Diego Zoo —Escondido, CA
- $130,421 - $146,724 a year
- Email
- Carpentry
- Hospitality
- Research
- Free parking
- Wellness program
7d
Associate Director, Enterprise Talent Management
Illumina —San Diego, CA
- $155,600 - $233,400 a year
- Full-time
- Hybrid work
- Background check
- 7 years
- Research
- Dental insurance
- Paid time off
12d
Senior Director, People & Culture
Salk Institute for Biological Studies —San Diego, CA
- $180,000 - $210,000 a year
- 5 years
- Office
- Bachelor's degree
- Health insurance
- Dental insurance
Senior Director Marketing
Adidas —Carlsbad, CA
- $172,900 - $238,500 a year
- Full-time
- Hybrid work
- Microsoft Excel
- Marketing
- English
- Paid parental leave
- Health savings account
6d
Associate Director of Public Relations
Illumina —San Diego, CA
- $155,600 - $233,400 a year
- Full-time
- Hybrid work
- Background check
- Office
- Travel
- Dental insurance
- Paid time off
6d
Senior Project Manager - Associate Director, CMC
CALIDI BIOTHERAPEUTICS INC —San Diego, CA
- $125,000 - $165,000 a year
- Full-time
- Bachelor of Science
- Basic math
- Laboratory experience
- Health insurance
- Dental insurance
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Associate Director, Learning and Capability Development
Illumina —San Diego, CA
- $155,600 - $233,400 a year
- Full-time
- Hybrid work
- Background check
- 7 years
- Continuous improvement
- Dental insurance
- Paid time off
12d
Associate Program Director, Flex & Hybrid Immersion
The University of St. Augustine for Health Sciences —San Marcos, CA
- $92,977 - $186,780 a year
- Doctoral degree
- Office
- Driver's License
- Paid holidays
- Disability insurance
Director/Senior Director, MSAT
Viking Therapeutics, Inc. —San Diego, CA
- $190,000 - $220,000 a year
- Writing skills
- 11+ years
- Analysis skills
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Director/Senior Director, Preclinical Pharmacology/Toxicology
Viking Therapeutics, Inc. —San Diego, CA
- $205,000 - $220,000 a year
- Writing skills
- Doctor of Philosophy
- Mentoring
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Senior Director, International Trade Compliance
General Atomics —Poway, CA
- $174,010 - $324,040 a year
- Extended hours
- 11+ years
- Travel
- Mentoring
- Relocation assistance
Senior Manager / Associate Director, CMC Project Management - Process Development & Validation
Artiva Biotherapeutics —San Diego, CA
- $155,000 - $190,000 a year
- Full-time
- Hybrid work
- 6 years
- Bachelor's degree
- Senior level
- Paid holidays
- Disability insurance
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Associate Director, HRBP - Commercial (San Diego / Hybrid)
Illumina —San Diego, CA
- $155,600 - $233,400 a year
- Full-time
- Hybrid work
- Background check
- 5 years
- Office
- Dental insurance
- Paid time off
5d
Senior Director Product Marketing - Golf
Adidas —Carlsbad, CA
- $172,900 - $238,500 a year
- Full-time
- Hybrid work
- Microsoft Excel
- Marketing
- Merchandising
- Paid parental leave
- Health savings account
6d
Associate Director of Development, University Advancement
California State University —San Marcos, CA
- Full-time
- Background check
- University
- In-person
- Paid holidays
- Health insurance
Director, Partner Service Delivery – Consumer Group
Intuit —San Diego, CA
- $196,500 - $340,000 a year
- Bachelor's degree
- Experience equivalent to degree accepted
- Senior level
Assistant Director/ Associate Director/ Director, Patient Safety Operations
Ionis Pharmaceuticals, Inc. —Carlsbad, CA
- $132,140 - $268,875 a year
- Hybrid work
- English
- Mentoring
- Senior level
Quick Apply
Associate Director, Biomarker Operations
Artiva Biotherapeutics —San Diego, CA
- $175,000 - $185,000 a year
- Full-time
- 6 years
- Master's degree
- Bachelor's degree
- Paid holidays
- Disability insurance
Quick Apply
8d

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Associate Director of Toxicology

Kelly Services -
Carlsbad, CA

Quick Apply

Job Details

Full-time
$175,000 - $250,000 a year

Benefits

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

Qualifications

FDA submissions
Biotechnology
Investigational new drug (IND) applications
Collaborative research
Pre-clinical study projects
Pharmaceutical company experience
Compliance documentation
Regulatory submission editing and review
Communication with regulatory authorities for clinical trials
Managing projects
Safety and toxicology data reporting
Cross-functional collaboration
Managing medical research teams
Pharmaceutical research experience
Project stakeholder communication
Cross-functional communication
Toxicology research projects

Full Job Description

Kelly® Science & Clinical is seeking an Associate Director of Toxicology for a direct hire opportunity with one of our clients, a commercial-stage biotechnology company in the San Diego, CA area. 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: San Diego Metropolitan area
Position Title: Associate Director, Toxicology
Salary range: 175,000-250,000/ year
Are you ready to help drive innovation at the cutting edge of RNA-targeted medicine and advanced gene technologies? Our client is renowned for pioneering advances in biotechnology, delivering transformative therapies for serious diseases with a growing portfolio of marketed products and an industry-leading pipeline in neurology, cardiology, and other high-impact areas. Financially robust and passionately patient-focused, we are well positioned to continue shaping the future of RNA medicines and gene editing solutions.
A leading commercial-stage biotechnology innovator, headquartered in the vibrant San Diego area, is seeking a skilled and driven Toxicologist to join its dynamic Preclinical Development team. This role offers the unique opportunity to shape the nonclinical safety strategy for a diverse portfolio of transformative drug candidates. The team thrives on scientific rigor, cross-disciplinary collaboration, and a passion for advancing novel therapies. Onsite presence in Carlsbad, CA is required.
Key Responsibilities

Serve as the nonclinical safety authority for cross-functional project teams, offering strategic guidance to drive candidate selection, risk assessment, and program progression.
Design, oversee, and interpret both GLP and non-GLP studies focused on nonclinical pharmacology and toxicology, leveraging external partners for execution.
Directly manage outsourced studies conducted at CROs, ensuring robust study designs, protocol and report review, proactive issue resolution, and adherence to project timelines.
Synthesize multidimensional nonclinical datasets—including pharmacology, toxicology, clinical pathology, and TK/PK data—to generate integrated safety assessments.
Create and implement regulatory and nonclinical toxicology strategies for assigned programs.
Prepare and critically review nonclinical content for key regulatory submissions (e.g., Investigator’s Brochures, INDs, NDAs, DSURs), and represent the company in global regulatory interactions.
Evaluate the significance of safety findings and mechanisms of toxicity, ensuring human relevance and impact on development goals.
Communicate essential nonclinical safety findings, risk evaluations, and implications to internal teams and governance stakeholders.
Build effective partnerships with both internal colleagues and external collaborators within a matrixed development framework.
Represent the organization’s interests externally through engagement with scientific meetings, industry consortia, working groups, and professional societies.
Make meaningful contributions to peer-reviewed scientific publications.

Qualifications

Advanced degree (Master’s or Ph.D.) in Toxicology or a related life science discipline.
A minimum of 8 years (with Master’s) or 5 years (with Ph.D.) of experience in nonclinical safety assessment within the pharmaceutical or biotechnology sector.
Demonstrated expertise in managing and overseeing CRO-conducted studies, with strong skills in protocol/report development and project management.
Deep experience in generating, integrating, and interpreting toxicological data to inform program decisions.
Proven ability to author high-quality regulatory documents, including IBs, INDs, CTDs, and other health authority submissions.
Strong leadership and communication skills, capable of influencing across matrixed R&D environments and engaging senior decision makers.
Passion for continuous professional growth and the advancement of toxicology expertise.
DABT certification is preferred.

Why Join Us:
Be a vital part of a trailblazing team where your contributions are valued and impactful. Embrace the opportunity to innovate in a collaborative and forward-thinking environment, advancing the future of treatment for neurological disorders.
If your qualifications align with the requirements of this role, we invite you to apply and take the next step in your career journey. Rest assured, even if this opportunity isn't the perfect match, your profile will remain within our network, ensuring you're connected to a wealth of future opportunities in the field of science and clinical research.
#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. 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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Refine Your Search

senior associate director jobs in carlsbad, ca

Associate Director of Toxicology

Senior Director, Business Transformation

Associate Director of Construction & Maintenance - San Diego Zoo Safari Park

Associate Director, Enterprise Talent Management

Senior Director, People & Culture

Senior Director Marketing

Associate Director of Public Relations

Senior Project Manager - Associate Director, CMC

Associate Director, Learning and Capability Development

Associate Program Director, Flex & Hybrid Immersion

Director/Senior Director, MSAT

Director/Senior Director, Preclinical Pharmacology/Toxicology

Senior Director, International Trade Compliance

Senior Manager / Associate Director, CMC Project Management - Process Development & Validation

Associate Director, HRBP - Commercial (San Diego / Hybrid)

Senior Director Product Marketing - Golf

Associate Director of Development, University Advancement

Director, Partner Service Delivery – Consumer Group

Assistant Director/ Associate Director/ Director, Patient Safety Operations

Associate Director, Biomarker Operations

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