Top 682 Associate director, medical writing 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
Quick Apply
Associate Director, Regulatory and Medical Writer
Ionis Pharmaceuticals, Inc. —Carlsbad, CA
- $142,588 - $201,472 a year
- Hybrid work
- 11+ years
- Bachelor's degree
- Mentoring
Quick Apply
Assistant Director / Associate Director, Pharmaceutical Development ‒ Regulatory Writing
Ionis Pharmaceuticals, Inc. —Carlsbad, CA
- $93,200 - $190,120 a year
- Hybrid work
- Bachelor of Science
- Bachelor's degree
- Doctor of Philosophy
Quick Apply
Associate Director, Medical Writing & Scientific Communications
Viking Therapeutics, Inc. —San Diego, CA
- $170,000 - $190,000 a year
- Medicine
- Microsoft Excel
- 5 years
Quick Apply
11d
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
Quick Apply
Associate Director, Medical Writing
Acadia Pharmaceuticals Inc. —San Diego, CA
- $157,000 - $196,500 a year
- 5 years
- Word processing
- Windows
- Paid parental leave
- Employee stock purchase plan
2d
Lecturer - EDMX 627: Assessment for Planning and Instruction (Fall 2026)
California State University —San Marcos, CA
- Temporary
- Background check
- School experience
- University
Associate Director Toxicology
Acadia Pharmaceuticals Inc. —San Diego, CA
- $155,000 - $193,200 a year
- Hybrid work
- 6 years
- Bachelor of Science
- Office
- Paid parental leave
- Employee stock purchase plan
Technical Writer
Viasat —Carlsbad, CA
- $82,000 - $153,000 a year
- Online Application
- Schematics
- Analysis skills
- Mentoring
External Communications Specialist
SOLV Energy, LLC —San Diego, CA
- $87,095 - $104,514 a year
- Full-time
- Marketing
- 5 years
- Mid-level
- Paid holidays
- Disability insurance
Quick Apply
Lecturer - EDRL 614A: Reading and Writing Assessment (Fall 2026)
California State University —San Marcos, CA
- Temporary
- Background check
- Classroom
- Doctoral degree
Technical Writer
Viasat, Inc. —Carlsbad, CA
- $82,000 - $153,000 a year
- Online Application
- Schematics
- Analysis skills
- Mentoring
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
8d
Associate Director of Development, University Advancement
California State University —San Marcos, CA
- Full-time
- Background check
- University
- In-person
- Paid holidays
- Health insurance
Management Analyst I - Sustainability
City of Encinitas —Encinitas, CA
- $82,659.20 - $116,313.60 a year
- Full-time
- Background check
- Current TB test
- Research
- AD&D insurance
- Disability insurance
2d
ASSOCIATE DIRECTOR, VOLUNTEER & DONOR ENGAGEMENT
The Scripps Research Institute —San Diego, CA
- $80,000 - $90,000 a year
- Office
- 3 years
- University
- Free parking
- Health savings account
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
2d
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
Principal Scientist / Senior Principal Scientist
Arisan Therapeutics, Inc —Carlsbad, CA
- $150,000 - $205,000 a year
- Full-time
- Analysis skills
- Doctor of Philosophy
- US work authorization
- Paid holidays
- Relocation assistance
Quick Apply
Associate Attorney - Medical Malpractice / General Liability Defense
Orion Placement —Del Mar, CA
- $125,000 - $155,000 a year
- Full-time
- Writing skills
- Mid-level
- 3 years
- Dental insurance
- Paid time off
Quick Apply

I want to receive the latest job alert for associate director, medical writing in carlsbad ca

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Explore jobs in more locations

associate director, medical writing jobs near carlsbad ca

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.

Quick Apply

Refine Your Search

associate director, medical writing jobs in carlsbad ca

Associate Director of Toxicology

Associate Director, Regulatory and Medical Writer

Assistant Director / Associate Director, Pharmaceutical Development ‒ Regulatory Writing

Associate Director, Medical Writing & Scientific Communications

Senior Project Manager - Associate Director, CMC

Associate Director, Medical Writing

Lecturer - EDMX 627: Assessment for Planning and Instruction (Fall 2026)

Associate Director Toxicology

Technical Writer

External Communications Specialist

Lecturer - EDRL 614A: Reading and Writing Assessment (Fall 2026)

Technical Writer

Associate Director, Learning and Capability Development

Associate Director of Development, University Advancement

Management Analyst I - Sustainability

ASSOCIATE DIRECTOR, VOLUNTEER & DONOR ENGAGEMENT

Associate Director of Public Relations

Assistant Director/ Associate Director/ Director, Patient Safety Operations

Principal Scientist / Senior Principal Scientist

Associate Attorney - Medical Malpractice / General Liability Defense

I want to receive the latest job alert for associate director, medical writing in carlsbad ca

Related Searches

Explore jobs in more locations

Job Seeker Tools

Employer Tools

Browse

Stay Connected